Haplogroup Q-M242: Difference between revisions
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{{Short description|Human Y chromosome DNA grouping common among Native Americans}} |
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{{About|the human Y-DNA haplogroup|the human mtDNA haplogroup|Haplogroup Q (mtDNA)}} |
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{{Infobox haplogroup |
{{Infobox haplogroup |
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|name=Q |
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| map |
|map=File:Global frequency distribution map of haplogroup Q-M242 (Y-DNA).png |
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|caption=Frequency distribution of haplogroup Q-M242.<ref name="pmid28251872">{{cite journal|last1=Balanovsky|first1=Oleg|last2=Gurianov|first2=Vladimir|last3=Zaporozhchenko|first3=Valery|last4=Balaganskaya|first4=Olga|last5=Urasin|first5=Vadim|last6=Zhabagin|first6=Maxat|last7=Grugni|first7=Viola|last8=Canada|first8=Rebekah|last9=Al-Zahery|first9=Nadia |last10=Raveane |first10=Alessandro|last11=Wen|first11=Shao-Qing|last12=Yan|first12=Shi|last13=Wang|first13=Xianpin|last14=Zalloua|first14=Pierre|last15=Marafi|first15=Abdullah|last16=Koshel|first16=Sergey|last17=Semino|first17=Ornella|last18=Tyler-Smith|first18=Chris|last19=Balanovska|first19=Elena|title=Phylogeography of human Y-chromosome haplogroup Q3-L275 from an academic/citizen science collaboration|journal=BMC Evolutionary Biology|date=February 2017|volume=17|issue=S1|pages=18|doi=10.1186/s12862-016-0870-2|pmid=28251872|pmc=5333174|bibcode=2017BMCEE..17S..18B|doi-access=free}}</ref> |
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| origin-date =17,000 to 22,000 years ago<ref name=Fagundes>{{cite journal |last= Fagundes |first= Nelson J.R. |coauthors= Ricardo Kanitz, Roberta Eckert, Ana C.S. Valls, Mauricio R. Bogo, Francisco M. Salzano, David Glenn Smith, Wilson A. Silva, Marco A. Zago, Andrea K. Ribeiro-dos-Santos, Sidney E.B. Santos, Maria Luiza Petzl-Erler, and Sandro L.Bonatto |title= Mitochondrial Population Genomics Supports a Single Pre-Clovis Origin with a Coastal Route for the Peopling of the Americas|url=http://www.familytreedna.com/pdf/Fagundes-et-al.pdf|format=pdf |journal= American Journal of Human Genetics |volume=82 |issue=3 |year=2008 |pages=583–592|accessdate=2009-11-19|quote=Since the first studies, it has been found that extant Native American populations exhibit almost exclusively five "mtDNA haplogroups" (A–D and X)6 classified in the autochthonous haplogroups A2, B2, C1, D1, and X2a.7 Haplogroups A–D are found all over the New World and are frequent in Asia, supporting a northeastern Asian origin of these lineages |doi= 10.1016/j.ajhg.2007.11.013 |pmid= 18313026 |pmc= 2427228}}</ref><ref name=Zegura>{{cite journal |pmid=14595095 |doi=10.1093/molbev/msh009 |url=http://mbe.oxfordjournals.org/cgi/reprint/21/1/164.pdf |title=High-Resolution SNPs and Microsatellite Haplotypes Point to a Single, Recent Entry of Native American Y Chromosomes into the Americas |year=2003 |last1=Zegura |first1=S. L. |journal=Molecular Biology and Evolution |volume=21 |pages=164–75 |last2=Karafet |first2=TM |last3=Zhivotovsky |first3=LA |last4=Hammer |first4=MF |issue=1}}</ref> |
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|origin-date=17,200 to 31,700 years ago<ref name=Fagundes>{{cite journal|first1=Nelson J. R.|last1=Fagundes|first2=Ricardo|last2=Kanitz|first3=Roberta|last3=Eckert|first4=Ana C. S.|last4=Valls|first5=Mauricio R.|last5=Bogo|first6=Francisco M.|last6=Salzano|first7=David Glenn|last7=Smith|first8=Wilson A.|last8=Silva|first9=Marco A.|last9=Zago |first10=Andrea K. |last10=Ribeiro-Dos-Santos|first11=Sidney E. B.|last11=Santos|first12=Maria Luiza|last12=Petzl-Erler|first13=Sandro L.|last13=Bonatto|title=Mitochondrial Population Genomics Supports a Single Pre-Clovis Origin with a Coastal Route for the Peopling of the Americas|url=http://www.familytreedna.com/pdf/Fagundes-et-al.pdf|journal=American Journal of Human Genetics|volume=82|issue=3|year=2008|pages=583–592|access-date=2009-11-19|quote=Since the first studies, it has been found that extant Native American populations exhibit almost exclusively five "mtDNA haplogroups" (A–D and X)6 classified in the autochthonous haplogroups A2, B2, C1, D1, and X2a.7 Haplogroups A–D are found all over the New World and are frequent in Asia, supporting a northeastern Asian origin of these lineages|doi=10.1016/j.ajhg.2007.11.013|pmid=18313026|pmc=2427228}}</ref><ref name=Zegura2004/><ref name="YFull-Experimental YTree">[http://www.yfull.com/tree/Q/ YFull YTree v4.02]</ref> (approximately 24,500 years BP) |
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| origin-place = [[Central Asia]],<ref>[http://www.isogg.org/tree/ISOGG_HapgrpQ.html Y-DNA Haplogroup Q and its Subclades - 2010]</ref> the [[Indian Subcontinent]],<ref name=Sharma07 /> [[Siberia]]<ref name=Genebase>{{cite web|title=Learn about Y-DNA Haplogroup Q |work=Wendy Tymchuk - Senior Technical Editor |url=http://www.genebase.com/tutorial/item.php?tuId=16|format=Verbal tutorial possible |publisher=Genebase Systems |year=2008|accessdate=2009-11-21|quote=Haplogroup Q, possibly the youngest of the 20 Y-chromosome haplogroups, originated with the SNP mutation M242 in a man from Haplogroup P that likely lived in Siberia approximately 15,000 to 20,000 years before present}}</ref> |
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|origin-place=[[Central Asia]],<ref name="2016ydna">[http://www.isogg.org/tree/ISOGG_HapgrpQ.html Y-DNA Haplogroup Q and its Subclades – 2016]</ref><ref name=Sharma2007/> [[South Central Siberia]]<ref name=Zegura2004/> |
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| ancestor = [[haplogroup P (Y-DNA)|P]] |
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|ancestor=[[haplogroup P (Y-DNA)|P1-M45]] |
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| descendants = Q1 (P36.2), Q* |
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|descendants= [[Haplogroup Q1|Q1]] (L232/S432) |
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| mutations = M242 |
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|mutations=M242 rs8179021 |
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| members =[[Indigenous peoples of the Americas|Indigenous Americans]], [[Kets]], and [[Selkups]] |
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|members= [[Ket people|Kets]] 93.8%,<ref name="Karafet2004">{{cite journal|last1=Karafet|first1=T. M.|year=2002|title=High Levels of Y-Chromosome Differentiation among Native Siberian Populations and the Genetic Signature of a Boreal Hunter-Gatherer Way of Life|journal=Human Biology|volume=74|issue=6|pages=761–789|doi=10.1353/hub.2003.0006|pmid=12617488|s2cid=9443804}}</ref> [[Indigenous peoples of South America]] 92%,<ref name="Bortolini2003"/> [[Inuit]] 80%,<ref>''Zegura Stephen L.'', ''Tatiana M. Karafet'', ''Lev A. Zhivotovsky'', ''Michael F. Hammer''. High-Resolution SNPs and Microsatellite Haplotypes Point to a Single, Recent Entry of Native American Y Chromosomes into the Americas, 2004.</ref> [[Turkmens]] from [[Karakalpakstan]] (mainly [[Yomut]]) 73%,<ref>https://www.researchgate.net/publication/310645015_Gene_pool_of_Turkmens_from_Karakalpakstan_in_their_Central_Asian_context_Y-chromosome_polymorphism{{full citation needed|date=February 2021}}</ref> [[Selkup people|Selkups]] 66.4%.,<ref name="Karafet2004"/> [[Altaians]] 63.6%.,<ref name="Kharkov2007">{{cite journal|last1=Kharkov|first1=V. N.|last2=Stepanov|first2=V. A.|last3=Medvedeva|first3=O. F.|last4=Spiridonova|first4=M. G.|last5=Voevoda|first5=M. I.|last6=Tadinova|first6=V. N.|last7=Puzyrev|first7=V. P.|year=2007|title=Gene Pool Differences between Northern and Southern Altaians Inferred from the Data on Y-Chromosomal Haplogroups|journal=Genetika|volume=43|issue=5|pages=675–687|pmid=17633562|doi=10.1134/S1022795407050110|s2cid=566825}}</ref> [[Tuvans]] (from [[Xinjiang]]) 62.5%.,<ref name = "Zhang2009">{{cite journal|last1=Yong-Ke|first1=Zhang|last2=Zheng|first2=Chen|last3=An|first3=FAN|display-authors=etal|year=2009|title=Genetic relationships between Tuva population and the neighboring populations in the Altai Region of Xinjiang Uygur Autonomous Region|journal=Yi Chuan = Hereditas|volume=31|issue=8|pages=818–824|doi=10.3724/SP.J.1005.2009.00818|pmid=19689942|s2cid=39635944|doi-access=free}}</ref> [[Chelkans]] 60.0%.,<ref name="Kharkov2007">{{cite journal|last1=Kharkov|first1=V. N.|last2=Stepanov|first2=V. A.|last3=Medvedeva|first3=O. F.|last4=Spiridonova|first4=M. G.|last5=Voevoda|first5=M. I.|last6=Tadinova|first6=V. N.|last7=Puzyrev|first7=V. P.|year=2007|title=Gene Pool Differences between Northern and Southern Altaians Inferred from the Data on Y-Chromosomal Haplogroups|journal=Genetika|volume=43|issue=5|pages=675–687|pmid=17633562|doi=10.1134/S1022795407050110|s2cid=566825}}</ref> [[Greenlandic Inuit]] 54%,<ref name=Olofsson2015/> [[Tubalar]] 41%,<ref name="Kharkov2007">{{cite journal|last1=Kharkov|first1=V. N.|last2=Stepanov|first2=V. A.|last3=Medvedeva|first3=O. F.|last4=Spiridonova|first4=M. G.|last5=Voevoda|first5=M. I.|last6=Tadinova|first6=V. N.|last7=Puzyrev|first7=V. P.|year=2007|title=Gene Pool Differences between Northern and Southern Altaians Inferred from the Data on Y-Chromosomal Haplogroups|journal=Genetika|volume=43|issue=5|pages=675–687|pmid=17633562|doi=10.1134/S1022795407050110|s2cid=566825}}</ref> [[Siberian Tatars]] ([[Ishtyak-Tokuz Tatars]]) 38%,<ref name="xn--c1acc6aafa1c.xn--p1ai">[http://xn--c1acc6aafa1c.xn--p1ai/?page_id=15461 Пять генофондов пяти субэтносов сибирских татар]</ref> the [[indigenous peoples of the Americas]], [[Akha people|Akha people of northern Thailand]], [[Mon-Khmer|Mon-Khmer people]], some [[tribes of Assam]] and [[Swati tribe]] of [[Pakistan]] |
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'''Haplogroup Q''' or '''Q-M242''' is a [[Human Y-chromosome DNA haplogroup|Y-chromosome DNA haplogroup]]. It has one primary [[subclade]], [[Haplogroup Q1]] (L232/S432), which includes numerous subclades that have been sampled and identified in males among modern populations. |
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Q-M242 is the predominant [[Y-DNA haplogroups in indigenous peoples of the Americas|Y-DNA haplogroup among Native Americans]], [[Swati tribe]] and several peoples of [[Central Asia]] and [[Far North (Russia)|Northern Siberia]]. |
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==Origins== |
==Origins== |
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[[Haplogroup]] Q-M242 is one of the two branches of [[Haplogroup P1 (Y-DNA)|P-P226 (M45)]], the other being [[Haplogroup R (Y-DNA)|R-M207]].<ref>{{Cite web|last=Estes|first=Roberta|date=2020-09-12|title=Y DNA Haplogroup P Gets a Brand-New Root – Plus Some Branches|url=https://dna-explained.com/2020/09/12/y-dna-haplogroup-p-gets-a-brand-new-root-plus-some-branches/|access-date=2024-01-21|website=DNAeXplained – Genetic Genealogy|language=en-US}}</ref> |
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[[Haplogroup]] Q is one of the two branches of [[Haplogroup P (Y-DNA)|haplogroup P]] (M45). Haplogroup Q is believed to have arisen in [[Central Asia]] or [[South Asia]] approximately 17,000 to 22,000 years ago.<ref name=karafet2008 /> It has had multiple origins proposed. Much of the conflict may be attributed to limited sample sizes and early definitions that used a combination of M242, P36.2, and MEH2 as defining mutations. |
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Q-M242 is believed to have arisen around the [[Altai Mountains]] area (or [[South Central Siberia]]),<ref name=Zegura2004/> approximately 17,000<ref name=Zegura2004/> to 31,700 years ago.<ref name="YFull-Experimental YTree"/> However, the matter remains unclear due to limited sample sizes and changing definitions of Haplogroup Q: early definitions used a combination of the [[Single-nucleotide polymorphism|SNPs]] M242, P36.2, and MEH2 as defining mutations. |
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This haplogroup has many diverse [[haplotype]]s despite its low frequency among most populations outside of the Americas. There also are over a dozen [[subclade]]s that have been sampled and identified in modern populations. |
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== |
==Technical specification of mutation== |
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The polymorphism, "M242", is a C→T transition residing in intron 1 (IVS-866) of the DBY gene and was discovered by Mark Seielstad et al. in 2003.<ref name="SeielstadYuldasheva2003">{{cite journal|last1=Seielstad|first1=Mark|last2=Yuldasheva|first2=Nadira|last3=Singh|first3=Nadia|last4=Underhill|first4=Peter|last5=Oefner|first5=Peter|last6=Shen|first6=Peidong|last7=Wells|first7=R. Spencer|title=A Novel Y-Chromosome Variant Puts an Upper Limit on the Timing of First Entry into the Americas|journal=The American Journal of Human Genetics|volume=73|issue=3|year=2003|pages=700–705|issn=0002-9297|doi=10.1086/377589|pmid=12929085|pmc=1180698}}</ref> |
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The technical details of M242 are: |
The technical details of M242 are: |
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:Position (base pair): 180 |
:Position (base pair): 180 |
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:Total size (base pairs): 366 |
:Total size (base pairs): 366 |
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:Forward 5′→ 3′: aactcttgataaaccgtgctg |
:Forward 5′→ 3′: {{DNA sequence|aactcttgataaaccgtgctg}} |
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:Reverse 5′→ 3′: tccaatctcaattcatgcctc |
:Reverse 5′→ 3′: {{DNA sequence|tccaatctcaattcatgcctc}} |
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==Subclades== |
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In [[Y chromosome]] phylogenetics, subclades are the branches of a haplogroup. These subclades are also defined by [[single-nucleotide polymorphism]]s (SNPs) or [[unique-event polymorphism]]s (UEPs). Haplogroup Q-M242, according to the most recent available [[phylogenetics]] has between 15 and 21 subclades. The scientific understanding of these subclades has changed rapidly. Many key SNPs and corresponding subclades were unknown to researchers at the time of publication are excluded from even recent research. This makes understanding the meaning of individual migration paths challenging. |
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===Phylogenetic trees=== |
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There are several confirmed and proposed [[phylogenetic tree]]s available for haplogroup Q-M242. The scientifically accepted one is the [[Y Chromosome Consortium]] (YCC) one published in Karafet 2008 and subsequently updated. A draft tree that shows emerging science is provided by Thomas Krahn at the Genomic Research Center in [[Houston]], [[Texas]]. The [[International Society of Genetic Genealogy]] (ISOGG) also provides an amateur tree. |
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====The 2015 ISOGG tree==== |
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== Subclades == |
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The [[subclade]]s of Haplogroup Q-M242 with their defining mutation (s), according to the 2015 ISOGG tree<ref name="2016ydna"/> are provided below. The first three levels of subclades are shown. Additional detail is provided on the linked branch article pages. |
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In Y-chromosome phylogenetics, subclades are the branches of haplogroups. These subclades are also defined by single nucleotide polymorphisms (SNPs) or unique event polymorphisms (UEPs). Haplogroup Q, according to the most recent available phylogenetics has between 15 and 21 subclades. The scientific understanding of these subclades has changed rapidly. Many key SNPs and corresponding subclades were unknown to researchers at the time of publication are excluded from even recent research. This makes understanding the meaning of individual migration paths challenging. |
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*'''Q-M242''' M242 |
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=== Haplogroup and Subclade Defining SNPs === |
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**'''Q-P36.2''' P36.2, L232, L273, L274 (Q1) |
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***'''Q-MEH2''' MEH2 (Q1a) |
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****'''Q-F1096''' F1096, F1215 (Q1a1) |
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*****'''[[Haplogroup Q-NWT01|Q-NWT01]]''' NWT01 (Q1a1a) |
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******'''[[Haplogroup Q-M120|Q-M120]]''' M120, M265/N14 (Q1a1a1) |
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*****'''[[Haplogroup Q-M25|Q-M25]]''' M25, M143 (Q1a1b) |
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******'''[[Haplogroup Q-L712 (Y-DNA)|Q-L712]]''' L712 (Q1a1b1) |
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****'''[[Haplogroup Q-M346|Q-M346]]''' L56, L57, M346, L528 (Q1a2) |
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*****'''[[Haplogroup Q-L53|Q-L53]]''' L53 (Q1a2a) |
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******'''[[Haplogroup Q-L54|Q-L54]]''' L54 (Q1a2a1) |
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*******'''[[Haplogroup Q-CTS11969 (Y-DNA)|Q-CTS11969]]''' CTS11969, M930 (Q1a2a1a) |
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********'''[[Haplogroup Q-M3|Q-M3]]''' M3 (Q1a2a1a1) |
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*********'''[[Haplogroup Q-M19 (Y-DNA)|Q-M19]]''' M19 (Q1a2a1a1a) |
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********'''[[Haplogroup Q-L804 (Y-DNA)|Q-L804]]''' L804 (Q1a2a1a2) |
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*******'''[[Haplogroup Q-CTS1780 (Y-DNA)|Q-CTS1780]]''' CTS1780, M981, M971, Z780 (Q1a2a1b) |
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*******'''[[Haplogroup Q-L330 (Y-DNA)|Q-L330]]''' L330 (Q1a2a1c) |
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*****'''[[Haplogroup Q-F835 (Y-DNA)|Q-F835]]''' F835, L940 (Q1a2b) |
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*****'''[[Haplogroup Q-F1161 (Y-DNA)|Q-F1161]]''' F1161 |
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******'''[[Haplogroup Q-L527 (Y-DNA)|Q-L527]]''' L527 |
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***'''[[Haplogroup Q-L275|Q-L275]]''' L275, L314 (Q2) |
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****'''[[Haplogroup Q-M378 (Y-DNA)|Q-M378]]''' M378/Page100, L214, L215/Page82 (Q2a) |
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*****'''[[Haplogroup Q-FGC1774 (Y-DNA)|Q-FGC1774]]''' FGC1774, Y2016 (Q1b1a) |
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******'''[[Haplogroup Q-L245 (Y-DNA)|Q-245]]''' L245 (Q1b1a1) |
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****'''[[Haplogroup Q-Y1150 (Y-DNA)|Q-Y1150]]''' Y1150 (Q1b2) (Q1b-L68) |
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====The Genomic Research Center draft tree==== |
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{|class="wikitable sortable" |
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Below is a 2012 tree by Thomas Krahn of the [[Genomic Research Center]].<ref>[http://ytree.ftdna.com/index.php?name=Draft&parent=31182976 Proposed Tree] {{webarchive|url=https://web.archive.org/web/20110711045430/http://ytree.ftdna.com/index.php?name=Draft&parent=31182976 |date=2011-07-11 }}</ref> The first three levels of subclades are shown. Additional detail is provided on the linked branch article pages.<ref name=ThomasDraftTree>{{cite web|url=http://ytree.ftdna.com/index.php?name=Draft&parent=root|title=FTDNA Draft Y-DNA Tree (AKA YTree)|last=Krahn|first=Thomas|publisher=[[Family Tree DNA]]|url-status=dead|archive-url=https://web.archive.org/web/20150815071342/http://ytree.ftdna.com/index.php?name=Draft|archive-date=2015-08-15}}</ref> |
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! Academic Name |
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! RS ID |
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*'''[[Haplogroup P (Y-DNA)|P-M45]]''' |
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! Position |
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**'''Q-M242''' M242 |
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! Change |
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*** P36.2, L232, L273.1, L274.1 |
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! YCC 2008 rev |
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**** [[Haplogroup Q-MEH2 (Y-DNA)|MEH2]], L472, L528 |
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! ISOGG 2008 |
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***** [[Haplogroup Q-M120|M120]], N14/M265 |
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! Parent Clade |
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***** [[Haplogroup Q-M25|M25]], M143, L714, L716 |
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! Publications |
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***** [[Haplogroup Q-M346|M346]], L56, L57, L474, L892, L942 |
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! Notes |
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***** [[Haplogroup Q-P89.1|P89.1]] |
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***** [[Haplogroup Q-NWT01|NWT01]] |
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**** [[Haplogroup Q-L275|L275]], L314, L606, L612 |
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***** [[Haplogroup Q-M378 (Y-DNA)|M378]], L214, L215 |
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====The Y Chromosome Consortium tree==== |
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This is the 2008 tree produced by the [[Y Chromosome Consortium]] (YCC).<ref name="karafet2008">{{cite journal|doi=10.1101/gr.7172008|title=New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree|year=2008|last1=Karafet|first1=T. M.|last2=Mendez|first2=F. L.|last3=Meilerman|first3=M. B.|last4=Underhill|first4=P. A.|last5=Zegura|first5=S. L.|last6=Hammer|first6=M. F.|journal=Genome Research|volume=18|issue=5|pages=830–8|pmid=18385274|pmc=2336805}}</ref> Subsequent updates have been quarterly and biannual. The current version is a revision of the 2010 update.<ref>{{cite web|url=https://www.familytreedna.com/y-dna-haplotree.aspx|title=Y-DNA Haplotree}} ''Family Tree DNA uses the Y-Chromosome Consortium tree and posts it on their website.''</ref> The first three levels of subclades are shown. Additional detail is provided on the linked branch article pages. |
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*'''[[Haplogroup P (Y-DNA)|P-M45]]''' |
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**'''Q-M242''' M242 |
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***'''Q-P36.2''' P36.2 |
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****'''[[Haplogroup Q-MEH2 (Y-DNA)|Q-MEH2]]''' MEH2 |
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******'''[[Haplogroup Q-M120|Q-M120]]''' M120, N14, M265 |
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******'''[[Haplogroup Q-M25|Q-M25]]''' M25, M143 |
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*****'''[[Haplogroup Q-M346|Q-M346]]''' L56, L57, M346 |
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******'''[[Haplogroup Q-P89.1|Q-P89.1]]''' P89.1 |
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****'''[[Haplogroup Q-L275|Q-L275]]''' L275 |
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*****'''[[Haplogroup Q-M378 (Y-DNA)|Q-M378]]''' L214, L215, M378 |
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===Phylogenetic variants=== |
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The subclade (under Q-MEH2) proposed by Sharma (2007), which shows polymorphism (ss4bp, rs41352448) at 72,314 position of human [[arylsulfatase]] D pseudogene, is not represented in any current trees under Q-MEH2.<ref>That is because it is a value for the [[Short tandem repeat|STR]] [[DYS435]] with a value of 8→9 within haplogroup Q-M242 and the trend is to include only binary markers in phylogenetic trees. However, these are from studies where all current branches of the Q-M242 tree have not been tested. The problematic phylogeny sampling of early studies has been demonstrated by subsequent studies that have found Q-M346, Q-M378, and Q-M25 in South Asia.</ref> The most plausible explanation for this could be an ancestral migration of individuals bearing Q-MEH2 to the Indian subcontinent followed by an [[Indigenous peoples|autochthonous differentiation]] to Q-ss4bp.<ref name=Sharma2007>{{cite journal|vauthors=Sharma S, Rai E, Bhat AK, Bhanwer AS, Bamezai RN|title=A novel subgroup Q5 of human Y-chromosomal haplogroup Q-M242 in India|journal=BMC Evol. Biol.|volume=7|pages=232|year=2007|pmid=18021436|pmc=2258157|doi=10.1186/1471-2148-7-232|issue=1|doi-access=free}}</ref> |
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==Distribution== |
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===Americas=== |
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{{Further|Genetic history of indigenous peoples of the Americas|Y-DNA haplogroups in indigenous peoples of the Americas}} |
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Several branches of haplogroup Q-M242 have been predominant [[Pre-Columbian era|pre-Columbian]] male lineages in [[indigenous peoples of the Americas]]. Most of them are descendants of the major founding groups who migrated [[Prehistoric migration and settlement of the Americas from Asia|from Asia into the Americas]] by crossing the [[Bering Strait]].<ref name=Zegura2004/> These small groups of founders must have included men from the [[Haplogroup Q-M346|Q-M346]], [[Haplogroup Q-L54|Q-L54]], [[Haplogroup Q-Z780|Q-Z780]], and [[Haplogroup Q-M3|Q-M3]] lineages. In North America, two other Q-lineages also have been found. These are [[Haplogroup Q-P89.1|Q-P89.1]] (under Q-MEH2) and [[Haplogroup Q-NWT01|Q-NWT01]]. They may have not been from the Beringia Crossings but instead come from later immigrants who traveled along the shoreline of Far East Asia and then the Americas using boats. |
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It is unclear whether the current frequency of Q-M242 lineages represents their frequency at the time of immigration or is the result of the shifts in a small founder population over time. Regardless, Q-M242 came to dominate the paternal lineages in the Americas. |
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====North America==== |
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In the indigenous people of North America, Q-M242 is found in [[Na-Dene languages|Na-Dené speakers]] at an average rate of 68%. The highest frequency is 92.3% in [[Navajo]], followed by 78.1% in [[Native Americans in the United States|Apache]],<ref name=Zegura2004>{{cite journal|pmid=14595095|doi=10.1093/molbev/msh009|title=High-Resolution SNPs and Microsatellite Haplotypes Point to a Single, Recent Entry of Native American Y Chromosomes into the Americas|year=2004|last1=Zegura|first1=S. L.|journal=Molecular Biology and Evolution|volume=21|pages=164–75|last2=Karafet|first2=TM|last3=Zhivotovsky|first3=LA|last4=Hammer|first4=MF|issue=1|doi-access=free}}</ref> 87%<ref name=Zegura2004/> in SC Apache,<ref name='Malhi2008'>{{cite journal|pmc=2584155|pmid=18618732|doi=10.1002/ajpa.20883|volume=137|issue=4|title=Distribution of Y chromosomes among native North Americans: a study of Athapaskan population history|year=2008|journal=Am. J. Phys. Anthropol.|pages=412–24|last1=Malhi|first1=RS|last2=Gonzalez-Oliver|first2=A|last3=Schroeder|first3=KB|last4=Kemp|first4=BM|last5=Greenberg|first5=JA|last6=Dobrowski|first6=SZ|last7=Smith|first7=DG|last8=Resendez|first8=A|last9=Karafet|first9=T | last10 = Hammer | first10 = M|last11=Zegura|first11=S|last12=Brovko|first12=T}}</ref> and about 80% in North American [[Eskimo]] ([[Inuit]], [[Yupik peoples|Yupik]])–[[Aleut]] populations. (Q-M3 occupies 46% among Q in North America)<ref name=genetree>{{cite web|title=Frequency Distribution of Y-DNA Haplogroup Q M3|url=http://www.genetree.com/education/q|publisher=GeneTree|year=2010|access-date=2010-01-30|url-status=dead|archive-url=https://web.archive.org/web/20091104070218/http://www.genetree.com/education/q|archive-date=2009-11-04}}</ref> |
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On the other hand, a 4000-year-old [[Saqqaq culture|Saqqaq]] individual belonging to Q1a-MEH2* has been found in [[Greenland]]. Surprisingly, he turned out to be genetically more closely related to Far East Siberians such as [[Koryaks]] and [[Chukchi people]] rather than Native Americans.<ref name=pmid20148029>{{cite journal|display-authors=8|last1=Rasmussen|first1=Morten|last2=Li|first2=Yingrui|last3=Lindgreen|first3=Stinus|last4=Pedersen|first4=Jakob Skou|last5=Albrechtsen|first5=Anders|last6=Moltke|first6=Ida|last7=Metspalu|first7=Mait|last8=Metspalu|first8=Ene|last9=Kivisild|first9=Toomas |last10=Gupta |first10=Ramneek|last11=Bertalan|first11=Marcelo|last12=Nielsen|first12=Kasper|last13=Gilbert|first13=M. Thomas P.|last14=Wang|first14=Yong|last15=Raghavan|first15=Maanasa|last16=Campos|first16=Paula F.|last17=Kamp|first17=Hanne Munkholm|last18=Wilson|first18=Andrew S.|last19=Gledhill|first19=Andrew |last20=Tridico |first20=Silvana|last21=Bunce|first21=Michael|last22=Lorenzen|first22=Eline D.|last23=Binladen|first23=Jonas|last24=Guo|first24=Xiaosen|last25=Zhao|first25=Jing|last26=Zhang|first26=Xiuqing|last27=Zhang|first27=Hao|last28=Li|first28=Zhuo|last29=Chen|first29=Minfeng |last30=Orlando |first30=Ludovic|last31=Kristiansen|first31=Karsten|last32=Bak|first32=Mads|last33=Tommerup|first33=Niels|last34=Bendixen|first34=Christian|last35=Pierre|first35=Tracey L.|last36=Grønnow|first36=Bjarne|last37=Meldgaard|first37=Morten|last38=Andreasen|first38=Claus|last39=Fedorova|first39=Sardana A. |last40=Osipova |first40=Ludmila P.|last41=Higham|first41=Thomas F. G.|last42=Ramsey|first42=Christopher Bronk|last43=Hansen|first43=Thomas v. O.|last44=Nielsen|first44=Finn C.|last45=Crawford|first45=Michael H.|last46=Brunak|first46=Søren|last47=Sicheritz-Pontén|first47=Thomas|last48=Villems|first48=Richard|last49=Nielsen|first49=Rasmus |last50=Krogh |first50=Anders|last51=Wang|first51=Jun|last52=Willerslev|first52=Eske|title=Ancient human genome sequence of an extinct Palaeo-Eskimo|journal=Nature|date=February 2010|volume=463|issue=7282|pages=757–762|doi=10.1038/nature08835|pmid=20148029|pmc=3951495|bibcode=2010Natur.463..757R}}</ref> Today, the frequency of Q runs at 53.7% (122/227: 70 Q-NWT01, 52 Q-M3) in [[Greenland]], showing the highest in east [[Sermersooq]] at 82% and the lowest in [[Qeqqata]] at 30%.<ref name=Olofsson2015>{{cite journal|last1=Katharina Olofsson|first1=Jill|display-authors=etal|year=2015|title=Peopling of the North Circumpolar Region – Insights from Y Chromosome STR and SNP Typing of Greenlanders|journal=PLOS One|volume=10|issue=1|pages=e0116573|doi=10.1371/journal.pone.0116573|pmid=25635810|pmc=4312058|bibcode=2015PLoSO..1016573O|doi-access=free}}</ref> |
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Q-M242 is estimated to occupy 3.1% of the whole US population in 2010:<ref name="uspop">{{cite journal|last1=Hammer|display-authors=etal|date=Dec 2006|title=Population structure of Y chromosome SNP haplogroups in the United States and forensic implications for constructing Y chromosome STR databases|journal=Forensic Sci. Int.|volume=164|issue=1|pages=45–55|doi=10.1016/j.forsciint.2005.11.013|pmid=16337103}}</ref> |
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{|class="wikitable" |
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!Ethnicity |
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!Percentage of USA population † |
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!Haplogroup Q frequency |
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|- |
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|White |
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| P48||-||13006660-13006661||–>T||Q1a4||Q1a4||MEH2||||This is now considered a private SNP. The positive sample from Karafet 2008 was retested at the [[FTDNA|Family Tree DNA]] GRC and was found to be negative. |
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|63.7% |
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|Q-P36* 0.6% & Q-M3 0.1% |
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|- |
|- |
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|Hispanic |
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| L57||rs34864948||14083496||A/G||-||-||P36.2|||| |
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|16.3% |
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| Q-P36* 3.8% & Q-M3 7.9% |
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|- |
|- |
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| Black |
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| L191||-||2947379||A>del||-||-||L53, L54, L55, L213, L331, L475, L476|||| The L191 SNP has been observed in several paternal lineages which are thought to have originated in northern Mexico. |
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|12.6% |
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|Q-P36* (xM3) 0.2% |
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|- |
|- |
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|Asian |
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| L213||rs34549365||8295033||C>G||-||-||L56, L57, L528, M346|||| |
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|4.8% |
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|~0% |
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|- |
|- |
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|Native American ‡ |
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| L245||-||5735090||C>G||-||-||M378, L214, L215|||| |
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| 0.9% |
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|Q-P36* 31.2% & Q-M3 26.9% |
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|- |
|- |
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|colspan=3|Source :<ref name="uspop"/> |
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| M346||-||2947156||C>G||Q1a3||Q1a3||MEH2|||| |
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|- |
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† According to the US National Population [[2010 United States Census|Census data (2010)]]<ref>[https://www.census.gov/popest/data/index.html Population Estimates] {{webarchive|url=https://web.archive.org/web/20141218204847/http://www.census.gov/popest/data/index.html |date=2014-12-18 }}</ref> |
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| L215|| [http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?searchType=adhoc_search&type=rs&rs=rs34601266 rs34601266] ||13399368||C>T||-||-||P36.2|||| |
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|- |
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‡ Mainland and Alaska, not including the Pacific islands |
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| L55||rs35768544||17922729||G>A||-||-||L56, L57, L528, M346|||| |
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|- |
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| L53||rs34724285||20101684||G>A||-||-||L56, L57, L528, M346|||| |
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|- |
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| L54||rs34954951||21702170||G>A||-||-||L56, L57, L528, M346|||| |
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|- |
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| L232||-||16025489||G>A||-||-||M242|||| The SNP was found during WTY testing at the [[FTDNA|Family Tree DNA]] GRC. |
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|- |
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| L56||rs34703625||8208869||G>A||-||-||P36.2|||| |
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|- |
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| P36.2||-||13006449||G>T||Q1||Q1||M242|||| |
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|- |
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| MEH2||[http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?searchType=adhoc_search&type=rs&rs=rs4252209 rs4252209]||4985637||G>T||Q1a||Q1a||P36.2|||| |
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|- |
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| L214|| [http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?searchType=adhoc_search&type=rs&rs=rs34694026 rs34694026] ||20365995||T>C||-||-||P36.2|||| |
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|- |
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| M3||rs3894||17605757||C>T||Q1a3a||Q1a3a||L53, L54, L55|||| The M3 SNP defines the dominant Y-DNA subclade of Haplogroup Q for the [[indigenous people of the Americas]]. This SNP is geographically widespread, occurring from the northeast tip of [[Siberia]] and throughout [[North America]], the [[Caribbean]], [[Central America]], and [[South America]]. |
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|- |
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| M194||rs2032677||13523944||T>C||Q1a3a2||Q1a3a2||M3|||| |
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|- |
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| P292||rs13447374||13540161||–>G||Q1a3a3||Q1a3a3||M3|||| |
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|- |
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| P106||-||13932316||G>A||Q1a3a3||Q1a3a3||M3|||| |
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|- |
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| M19||rs3910||20192619||T>A||Q1a3a1||Q1a3a1||M3|||| |
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|- |
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| M199||rs2032589||13540505-13540504||–>G||Q1a3a3||Q1a3a3||M3|||| |
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|- |
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| M323||rs13447377||20327106||C>T||Q1a6||Q1a6||M346|||| |
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|- |
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| P89.1||-||13359859||G>T||Q1a5||Q1a5||MEH2||||Limited research indicates that this may be a private SNP. The P89 mutation is also found in R1b. |
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|- |
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| M265, N14||rs3212294||13540044||C>A||Q1a1||Q1a1||MEH2|||| |
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|- |
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| M242||rs8179021||13527976||C>T||Q||Q||P SNPs|||| |
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|- |
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| M378||-||13536901||A>G||Q1b||Q1b||P36.2|||| |
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|- |
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| M25||-||20326052||G>C||Q1a2||Q1a2||P36.2|||| |
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|- |
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| M143||-||20349206||G>T||Q1a2||Q1a2||P36.2|||| |
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|- |
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| M120||-||20366782||T>C||Q1a1||Q1a1||P36.2|||| |
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|} |
|} |
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====Mesoamerica & South America==== |
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=== Phylogenetic Variants === |
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Haplogroup Q-M242 has been found in approximately 94% of [[Indigenous peoples of the Americas|Indigenous peoples]] of [[Mesoamerica]] and [[South America]].<ref name="Bortolini2003">{{cite journal|last1=Bortolini|first1=Maria-Catira|last2=Salzano|first2=Francisco M.|last3=Thomas|first3=Mark G.|last4=Stuart|first4=Steven|last5=Nasanen|first5=Selja P.K.|last6=Bau|first6=Claiton H.D.|last7=Hutz|first7=Mara H.|last8=Layrisse|first8=Zulay|last9=Petzl-Erler|first9=Maria L. |last10=Tsuneto |first10=Luiza T.|last11=Hill|first11=Kim|last12=Hurtado|first12=Ana M.|last13=Castro-de-Guerra|first13=Dinorah|last14=Torres|first14=Maria M.|last15=Groot|first15=Helena|last16=Michalski|first16=Roman|last17=Nymadawa|first17=Pagbajabyn|last18=Bedoya|first18=Gabriel|last19=Bradman|first19=Neil |last20=Labuda |first20=Damian|last21=Ruiz-Linares|first21=Andres|title=Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas|journal=The American Journal of Human Genetics|date=September 2003|volume=73|issue=3|pages=524–539|doi=10.1086/377588|pmid=12900798|pmc=1180678|display-authors=8}}</ref> |
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The subclade proposed by Sharma 2007 (SS4bp, rs41352448) is not represented in any current trees because it is a value for the [[Short tandem repeat|STR]] [[DYS435]] with a value of 12.<ref name=Sharma07/> Karafet 2008, dismissed it as unsuitable by not including it on the Y-Chromosome Consortium tree.<ref name="karafet2008">{{cite journal |doi=10.1101/gr.7172008 |title=New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree |year=2008 |last1=Karafet |first1=T. M. |last2=Mendez |first2=F. L. |last3=Meilerman |first3=M. B. |last4=Underhill |first4=P. A. |last5=Zegura |first5=S. L. |last6=Hammer |first6=M. F. |journal=Genome Research |volume=18 |issue=5 |pages=830–8 |pmid=18385274 |pmc=2336805}}</ref> It has also been determined to be unsuitable for inclusion on the [[ISOGG]] Y-DNA tree.<ref>Private communication reported between Charles Moore, of ISOGG, and Rebekah Adele Canada, of the FTDNA Y-DNA Q Project.</ref> Further, analysis of STR based haplotypes from Sharma 2007 indicates that the DYS435=12 variant, using online haplogroup prediction tools, may occur in multiple branches of the Q tree. |
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The frequencies of Q among the whole male population of each country reach as follows: |
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===Phylogenetic Trees=== |
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* 61% in [[Bolivia]].<ref>{{cite journal|last1=Vullo|first1=Carlos|display-authors=etal|year=2014|title=Association between Y haplogroups and autosomal AIMs reveals intra-population substructure in Bolivian populations|journal=Int J Legal Med|volume=129|issue=4|pages=673–680|doi=10.1007/s00414-014-1025-x|pmid=24878616|s2cid=2906322}}</ref> |
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There are several confirmed and proposed phylogenetic trees available for haplogroup Q. The scientifically accepted one is the Y-Chromosome Consortium (YCC) one published in Karafet 2008 and subsequently updated. A draft tree that shows emerging science is provided by Thomas Krahn at the Genomic Research Center in [[Houston, Texas]]. The International Society of Genetic Genealogy (ISOGG) also provides an amateur tree. |
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* 51% in [[Guatemala]],<ref>{{cite journal|last1=Söchtig|first1=Jens|display-authors=etal|year=2015|title=Genomic insights on the ethno-history of the Maya and the 'Ladinos' from Guatemala|journal=BMC Genomics|volume=16|issue=1|page=131|doi=10.1186/s12864-015-1339-1|pmid=25887241|pmc=4422311|doi-access=free}} => Guatemala population consists of about 40% Tribal Natives (Mayans)+60% Native (Spanish Speaking). According to this paper, 89% of Mayan and 25% of Ladinos belong to Y-DNA Q. Thus, 40*0.89+60*0.25=50.6%</ref> |
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* 40.1% (159/397)<ref name="Battaglia2013"/> to 50% in [[Peru]] |
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* 37.6% in [[Ecuador]],<ref>{{cite journal|last1=Gaviria|first1=A.|display-authors=etal|year=2013|title=Characterization and Haplotype analysis of 11 Y-STR loci in Ecuadorian population|journal=Forensic Sci. Int. Genet. Suppl.|volume=4|issue=1|pages=e310–e311|doi=10.1016/j.fsigss.2013.10.158}}</ref> |
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* 37.3% (181/485) in [[Mexico]]<ref name="Battaglia2013">{{cite journal|last1=Battaglia|display-authors=etal|year=2013|title=The First Peopling of South America: New Evidence from Y-Chromosome Haplogroup Q|journal=PLOS One|volume=8|issue=8|pages=e71390|doi=10.1371/journal.pone.0071390|pmid=23990949|pmc=3749222|bibcode=2013PLoSO...871390B|doi-access=free}}</ref> (30.8% (203/659) among the specifically [[Mestizo]] segment)<ref>{{cite journal|last1=Martínez-Cortés|first1=G|display-authors=etal|year=2012|title=Admixture and population structure in Mexican-Mestizos based on paternal lineages|journal=J. Hum. Genet.|volume=57|issue=9|pages=568–74|pmid=22832385|doi=10.1038/jhg.2012.67|doi-access=free}}</ref> |
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* 31.2% (50/160) in [[El Salvador]],<ref>{{cite journal|last1=Lovo-Gómez|first1=J|display-authors=etal|date=Sep 2007|title=The genetic male legacy from El Salvador|journal=Forensic Sci. Int.|volume=171|issue=2–3|pages=198–203|doi=10.1016/j.forsciint.2006.07.005|pmid=16916590}}</ref> |
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* 15.3% (37/242) to 21.8% (89/408) in [[Panama]],<ref name="Battaglia2013"/><ref>{{cite journal|last1=Grugni|year=2015|title=Exploring the Y Chromosomal Ancestry of Modern Panamanians|journal=PLOS One|volume=10|issue=12|pages=e0144223|doi=10.1371/journal.pone.0144223|pmid=26636572|pmc=4670172|bibcode=2015PLoSO..1044223G|doi-access=free}}</ref> |
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* 16.1% in [[Colombia]],<ref>{{cite journal|last1=Rojas|first1=Win|display-authors=etal|year=2010|title=Genetic Make Up and Structure of Colombian Populations by Means of Uniparental and Biparental DNA Markers|journal=American Journal of Physical Anthropology|volume=143|issue=1|pages=13–20|doi=10.1002/ajpa.21270|pmid=20734436}}=> (DANE, 2006) 86% of the whole Colombian population self-reported as of Mixed Ancestry, 3.4% as Native American, 10.5% as African-Columbian. In this paper, 12% (114/954) of MA, 95.7% (135/141) of NA, and 23.8% (5/21) of AC are turned out to be Y-DNA Q. Thus, 86*0.12+3.4*0.957+10.5*0.238=16.1%</ref> |
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* 15.2% (25/165) in [[Nicaragua]],<ref>{{cite journal|last1=Núñez|first1=Carolina|display-authors=etal|year=2012|title=Y chromosome haplogroup diversity in a Mestizo population of Nicaragua|doi=10.1016/j.fsigen.2012.06.011|pmid=22770600|journal=Forensic Sci. Int. Genet.|volume=6|issue=6|pages=e192–e195}} The author revised his previous paper, genotyping 2 more samples as haplogroup Q by Y-SNP test.</ref> |
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* 9.7% (20/206) in [[Chile]],<ref name="Battaglia2013"/> |
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* 5.3% (13/246 in 8 provinces in northeastern, central, southern regions)<ref>{{cite journal|last1=Corach|first1=Daniel|display-authors=etal|year=2010|title=Inferring Continental Ancestry of Argentineans from Autosomal, Y-Chromosomal and Mitochondrial DNA|journal=Annals of Human Genetics|volume=74|issue=1|pages=65–76|doi=10.1111/j.1469-1809.2009.00556.x|pmid=20059473|hdl=11336/14301|s2cid=5908692|hdl-access=free}}</ref> to 23.4% (181/775 in 8 provinces in central-west, central, northwest regions)<ref>{{cite journal|last1=Ramallo|display-authors=etal|date=Dec 2009|title=Comparison of Y-chromosome haplogroup frequencies in eight Provinces of Argentina|journal=Forensic Science International: Genetics Supplement Series|volume=2|issue=1|pages=431–432|doi=10.1016/j.fsigss.2009.08.047}}</ref> in [[Argentina]], |
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* 5% in [[Costa Rica]],<ref>{{cite journal|last1=Villalta|first1=M.|last2=Rodriguez|first2=A.|last3=González|first3=L.|last4=Arce|first4=V.|last5=Arrieta|first5=G.|last6=Morales|first6=A.|last7=Gusmão|first7=L.|last8=Espinoza|first8=M.|title=Haplotype data for 12 Y-chromosome STR loci from Costa Rica|journal=Forensic Science International: Genetics Supplement Series|date=August 2008|volume=1|issue=1|pages=252–254|doi=10.1016/j.fsigss.2007.10.101|doi-access=free}}</ref> |
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* 3.95% in [[Brazil]],<ref>{{cite journal|last1=Palha|first1=T.|display-authors=etal|year=2012|title=Disclosing the Genetic Structure of Brazil through Analysis of Male Lineages with Highly Discriminating Haplotypes|journal=PLOS One|volume=7|issue=7|page=e40007|doi=10.1371/journal.pone.0040007|pmid=22808085|pmc=3393733|bibcode=2012PLoSO...740007P|doi-access=free}}=> about 80 out of 2,024 (3.95%) samples in the paper collected from all the regions of [[Brazil]] can be classified as Y-DNA Q.</ref> and so on. |
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===Asia=== |
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==== The Genomic Research Center Draft Tree ==== |
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Q-M242 originated in [[Asia]] (Altai region), and is widely distributed across it.<ref name=Zegura2004/> Q-M242 is found in Russia, [[Siberia]] ([[Ket people|Kets]],<ref name="Karafet2004"/> [[Selkup people|Selkups]], [[Siberian Yupik people]], [[Nivkh people|Nivkhs]], [[Chukchi people]],<ref name=Lell2002/> [[Yukaghir people|Yukaghirs]], [[Tuvans]],<ref name="Pakendorf2006">{{cite journal|last1=Pakendorf|first1=Brigitte|last2=Novgorodov|first2=Innokentij N.|last3=Osakovskij|first3=Vladimir L.|last4=Danilova|first4=Al’Bina P.|year=2006|last5=Protod’Jakonov|first5=Artur P.|last6=Stoneking|first6=Mark|title=Investigating the effects of prehistoric migrations in Siberia: genetic variation and the origins of Yakuts|journal=Human Genetics|volume=120|issue=3|pages=334–353|doi=10.1007/s00439-006-0213-2|pmid=16845541|s2cid=31651899}}</ref> [[Altai people]],<ref name="Kharkov2007"/> [[Koryaks]], etc.), [[Mongolia]],<ref name="Hammer2005">{{cite journal|doi=10.1007/s10038-005-0322-0|title=Dual origins of the Japanese: Common ground for hunter-gatherer and farmer Y chromosomes|year=2005|last1=Hammer|first1=Michael F.|last2=Karafet|first2=Tatiana M.|last3=Park|first3=Hwayong|last4=Omoto|first4=Keiichi|last5=Harihara|first5=Shinji|last6=Stoneking|first6=Mark|last7=Horai|first7=Satoshi|journal=Journal of Human Genetics|volume=51|pages=47–58|pmid=16328082|issue=1|doi-access=free}}</ref> China,<ref name="BoWen2004"/><ref name="BingSuHimalaya">{{cite journal|doi=10.1007/s004390000406|title=Y chromosome haplotypes reveal prehistorical migrations to the Himalayas|year=2000|last1=Su|first1=Bing|last2=Xiao|first2=Chunjie|last3=Deka|first3=Ranjan|last4=Seielstad|first4=Mark T.|last5=Kangwanpong|first5=Daoroong|last6=Xiao|first6=Junhua|last7=Lu|first7=Daru|last8=Underhill|first8=Peter|last9=Cavalli-Sforza|first9=Luca|last10=Chakraborty|first10=Ranajit|last11=Jin|first11=Li|journal=Human Genetics|volume=107|issue=6|pages=582–90|pmid=11153912|s2cid=36788262|display-authors=8}}</ref> [[Uyghurs]],<ref name="Hammer2005"/> [[Tibet]],<ref name="Gayden2007">{{cite journal|last1=Gayden|first1=Tenzin|display-authors=etal|date=May 2007|title=The Himalayas as a Directional Barrier to Gene Flow|journal=The American Journal of Human Genetics|volume=80|issue=5|pages=884–894|doi=10.1086/516757|pmid=17436243|pmc=1852741}}</ref> [[Korea]], Japan, [[Indonesia]],<ref name="Kim2011"/> [[Vietnam]],<ref name = "Karafet2010" /> [[Thailand]],<ref name=Trejaut2014/> India,<ref name="ycc">{{Cite web|url=http://ycc.biosci.arizona.edu/new_binary_polymorphism/resultsanddiscussions.html|title=The Y Chromosome Consortium 2008|access-date=2010-07-17|archive-url=https://archive.today/20080922062230/http://ycc.biosci.arizona.edu/new_binary_polymorphism/resultsanddiscussions.html|archive-date=2008-09-22|url-status=dead}}</ref> [[Pakistan]],<ref name="ycc" /> [[Afghanistan]], [[Iran]],<ref name="Cristofaro2013">{{cite journal|last1=Cristofaro|display-authors=etal|year=2013|title=Afghan Hindu Kush: Where Eurasian Sub-Continent Gene Flows Converge|journal=PLOS One|volume=8|issue=10|pages=e76748|doi=10.1371/journal.pone.0076748|pmid=24204668|pmc=3799995|bibcode=2013PLoSO...876748D|doi-access=free}}</ref> [[Iraq]], [[Saudi Arabia]], [[Turkmenistan]], [[Uzbekistan]], and so on. (For details, see below.) |
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This is Thomas Krahn at the Genomic Research Center's Draft tree [http://ytree.ftdna.com/index.php?name=Draft&parent=31182976 Proposed Tree] for haplogroup Q. |
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====North Asia==== |
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*'''[[Haplogroup P (Y-DNA)|P]]''' |
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In [[Siberia]], the regions between [[Altai Mountains|Altai]] and [[Lake Baikal]], which are famous for many prehistoric cultures and as the most likely birthplace of haplogroup Q, exhibit high frequencies of Q-M242. In a study (Dulik 2012),<ref name="Dulik2012">{{cite journal|last1=Dulik|first1=M C|date=Feb 2012|title=Mitochondrial DNA and Y Chromosome Variation Provides Evidence for a Recent Common Ancestry between Native Americans and Indigenous Altaian|journal=The American Journal of Human Genetics|volume=90|issue=2|pages=229–246|doi=10.1016/j.ajhg.2011.12.014|pmid=22281367|pmc=3276666}}</ref> Q-M242 (mostly Q-M346 including some Q-M3) has been found in 24.3% (46/189: 45 Q-M346, 1 Q-M25) of all Altaian samples. Among them, [[Chelkans]] show the highest frequency at 60.0% (15/25: all Q-M346), followed by [[Tubalar]]s at 41% (11/27: 1 Q-M25, 10 Q-M346) and Altaians-Kizhi at 17% (20/120). |
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**'''Q''' M242 |
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In a former study, Q-M242 is found in 4.2% of southern [[Altai people|Altaians]] and 32.0% of northern Altaians with the highest frequency of 63.6% in Kurmach-Baigol (Baygol). The frequency reaches 13.7% (20/146) in the whole samples.<ref name="Kharkov2007">{{cite journal|last1=Kharkov|first1=V. N.|last2=Stepanov|first2=V. A.|last3=Medvedeva|first3=O. F.|last4=Spiridonova|first4=M. G.|last5=Voevoda|first5=M. I.|last6=Tadinova|first6=V. N.|last7=Puzyrev|first7=V. P.|year=2007|title=Gene Pool Differences between Northern and Southern Altaians Inferred from the Data on Y-Chromosomal Haplogroups|journal=Genetika|volume=43|issue=5|pages=675–687|pmid=17633562|doi=10.1134/S1022795407050110|s2cid=566825}}</ref> In another study,<ref name= 'Malyarchuk2011'>{{cite journal|last1=Malyarchuk|first1=Boris|display-authors=etal|year=2011|title=Ancient links between Siberians and Native Americans revealed by subtyping the Y chromosome haplogroup Q1a|journal=Journal of Human Genetics|volume=56|issue=8|pages=583–588|doi=10.1038/jhg.2011.64|pmid=21677663|doi-access=free}}</ref> the frequency rises up to 25.8% (23/89: all Q-M346) in Altaians. Based on the results of these studies, the average frequency of Q-M242 in Altaians is about 21%. |
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*** P36.2, L232, L273, L274 |
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**** MEH2, L472, L528 |
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***** M120, N14, M265 |
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***** M25, M143 |
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****** L697.2, L712, L713, L714, L715, L716, M365.3 |
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***** M346, L56, L57, L474 |
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****** L53, L54, L55, L213, L331 |
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******* M3, L892 |
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******** M19 |
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******** M194 |
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******** M199, P106, P292 |
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******** PAGES00104, PAGES00126 |
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******** PAGES00131 |
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******** L663 |
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******** SA01 |
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******** L766, L767 |
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******** L883, L884, L885, L886, L887 |
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******** L888, L889, L890, L891 |
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******* L191 |
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******* L330, L334 |
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******** L329, L332, L333 |
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******* L400, L401 |
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******* L456 |
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******* L568, L569, L570, L571 |
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******** L567 |
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******** L619.1 |
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******* L804, L805 |
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******** L807 |
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****** M323 |
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****** L527, L529, L639 |
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****** L717, L718 |
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***** P89.1 |
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**** L275, L314 |
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***** M378, L214, L215 |
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****** L245 |
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******* L272.1 |
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******* L315 |
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******* L619.2 |
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****** L301 |
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****** L327 |
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[[Tuvan People's Republic|Tuva]], which is located on the east side of [[Altai Republic]] and west of [[Lake Baikal]] as well as on the north side of Mongolia, shows higher frequency of Q-M242. It is found in 14%<ref name = "Kharkov2012">[http://www.medgenetics.ru/UserFile/File/Doc/Diss_sovet/Vladimir%20Kharkov.pdf KHARKOV, Vladimir Nikolaevich, "СТРУКТУРА И ФИЛОГЕОГРАФИЯ ГЕНОФОНДА КОРЕННОГО НАСЕЛЕНИЯ СИБИРИ ПО МАРКЕРАМ Y-ХРОМОСОМЫ," ''Genetika'' 03.02.07 and "АВТОРЕФЕРАТ диссертации на соискание учёной степени доктора биологических наук," Tomsk 2012]</ref>~38.0% (41/108)<ref name=Malyarchuk2011/> of [[Tuvans]]. Also, Todjins ([[Tozhu Tuvans]]) in eastern Tuva show the frequency at ≤22.2% (8/36 P(xR1)<ref name = "Derenko2006">{{cite journal|last1=Derenko|first1=Miroslava|last2=Malyarchuk|first2=Boris|last3=Denisova|first3=Galina A.|display-authors=etal|year=2006|title=Contrasting patterns of Y-chromosome variation in South Siberian populations from Baikal and Altai-Sayan regions|journal=Hum Genet|volume=118|issue=5|pages=591–604|doi=10.1007/s00439-005-0076-y|pmid=16261343|s2cid=23011845}}</ref>)~38.5% (10/26, all Q-M346(xM3)).<ref name=Malyarchuk2011/> So, the average frequency of Q-M242 among Tuvans-Todjins in Tuva Republic is about 25%. Haplogroup Q-M242 has been found in 5.9% (3/51) of a sample of Tuvans from the village of Kanasi, 9.8% (5/51) of a sample of Tuvans from the village of Hemu, and 62.5% (30/48) of a sample of Tuvans from the village of Baihaba in northern [[Xinjiang]] near the international border with [[Altai Republic]].<ref name = "Zhang2009">{{cite journal|last1=Yong-Ke|first1=Zhang|last2=Zheng|first2=Chen|last3=An|first3=FAN|display-authors=etal|year=2009|title=Genetic relationships between Tuva population and the neighboring populations in the Altai Region of Xinjiang Uygur Autonomous Region|journal=Yi Chuan = Hereditas|volume=31|issue=8|pages=818–824|doi=10.3724/SP.J.1005.2009.00818|pmid=19689942|s2cid=39635944|doi-access=free}}</ref> |
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==== The Y-Chromosome Consortium tree ==== |
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This is the official scientific tree produced by the Y-Chromosome Consortium (YCC). The last major update was in 2008.<ref name=karafet2008 /> Subsequent updates have been quarterly and biannual. The current version is a revision of the 2010 update.<ref>{{cite web |url=https://www.familytreedna.com/y-dna-haplotree.aspx |title=Y-DNA Haplotree }} ''Family Tree DNA uses the Y-Chromosome Consortium tree and posts it on their website.''</ref> |
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In [[Siberian Tatars]], the [[Ishtyako-Tokuz]] sub-group of Tobol-Irtysh group has a frequency of Q-M242 at 38%.<ref name="xn--c1acc6aafa1c.xn--p1ai">[http://xn--c1acc6aafa1c.xn--p1ai/?page_id=15461 Пять генофондов пяти субэтносов сибирских татар]</ref> |
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*'''[[Haplogroup P (Y-DNA)|P]]''' |
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**'''Q''' M242 |
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***'''Q1''' P36.2 |
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****'''Q1a''' MEH2 |
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*****'''Q1a1''' M120, N14, M265 |
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*****'''Q1a2''' M25, M143 |
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*****'''Q1a3''' L213, L53, L54, L55 |
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******'''Q1a3a''' L56, L57, M346 |
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*******'''Q1a3a1''' M3 |
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********'''Q1a3a1a''' M19 |
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********'''Q1a3a1b''' M194 |
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********'''Q1a3a1c''' M199, P106, P292 |
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*******'''Q1a3a2''' L191 |
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******'''Q1a3b''' M323 |
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*****'''Q1a4''' P89.1 |
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****'''Q1b''' L275 |
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*****'''Q1b1''' L214, L215, M378 |
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******'''Q1b1a''' L272.1 |
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The highest frequencies of Q-M242 in Eurasia are witnessed in [[Ket people|Kets]] (central Siberia) at 93.8% (45/48) and in [[Selkup people|Selkups]] (north Siberia) at 66.4% (87/131).<ref name="Karafet2004"/> Russian ethnographers believe that their ancient places were farther south, in the area of the [[Altai Mountains|Altai]] and [[Sayan Mountains]]<ref name=Zegura2004/> ([[Altai-Sayan region]]). Their populations are currently small in number, being just under 1,500 and 5,000 respectively. In [[linguistic anthropology]], the Ket language is significant as it is currently the only surviving one in the [[Yeniseian languages|Yeniseian language family]] which has been linked by some scholars to the [[Indigenous peoples of the Americas|Native American]] [[Na-Dené languages]]<ref>E. J. VAJDA, "Siberian Link with Na-Dene Languages." The Dene–Yeniseian Connection, ed. by J. Kari and B. Potter(2010), pp.33–99, Anthropological Papers of the University of Alaska, new series, vol. 5(2010), Fairbanks: University of Alaska Fairbanks, Department of Anthropology</ref> and, more controversially, the [[Hunnic language|language of the Huns]]. (See: L. Lieti, E. Pulleybank,<ref>E. G. Pulleyblank, "The consonontal system of old Chinese" [Pt 1], Asia Major, vol. IX (1962), pp. 1–2</ref> [[Edward Vajda|E. Vajda]],<ref>E. J. Vajda, Yeniseian Peoples and Languages: A History of Yeniseian Studies with an Annotated Bibliography and a Source Guide (2013, Oxford/New York, Routledge) pp.103-106, etc.</ref> A. Vovin,<ref>{{cite journal|year=2000|title=Did the Xiong-nu speak a Yeniseian language?|journal=Central Asiatic Journal|volume=44|issue=1|pages=87–104}}</ref> etc.) |
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==== The 2011 ISOGG Tree ==== |
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Q-M346 is also found at lower rates in Sojots (7.1%, Q-M346), [[Khakas people|Khakassians]] (6.3%, Q-M346), [[Kalmyk people|Kalmyks]] (3.4%, Q-M25, Q-M346)<ref name=Malyarchuk2011/> and [[Khanty people|Khanty]],<ref name="Mirabal2009">{{cite journal|vauthors=Mirabal S, Regueiro M, Cadenas AM|display-authors=etal|title=Y-Chromosome distribution within the geo-linguistic landscape of northwestern Russia|journal=Eur. J. Hum. Genet.|volume=17|issue=10|pages=1260–73|date=March 2009|pmid=19259129|pmc=2986641|doi=10.1038/ejhg.2009.6}}</ref> and so on. |
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The [[subclade]]s of Haplogroup Q with their defining mutation(s), according to [http://www.isogg.org/tree/ISOGG_HapgrpQ.html the 2011 ISOGG tree] are provided below. |
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In far eastern Siberia, Q-M242 is found in 35.3% of [[Nivkh people|Nivkhs]] (Gilyaks) in the lower [[Amur River]], and 33.3% of [[Chukchi people]] and 39.2% of [[Siberian Yupik people]] in Chukotka ([[Chukchi Peninsula]]).<ref name=Lell2002>{{cite journal|last1=Jeffrey|first1=T.|display-authors=etal|date=Jan 2002|title=The Dual Origin and Siberian Affinities of Native American Y Chromosomes|journal=The American Journal of Human Genetics|volume=70|issue=1|pages=192–206|doi=10.1086/338457|pmid=11731934|pmc=384887}} The SNPs used in the paper are P-M45, R1a1-M17, Q1a2-M3, and other xP-M45 SNPs. And the author mentions that, among ethnic groups in the paper, R1-M173 is harbored only in some eastern Siberian Udegeys and Koryaks and Native Americans. Also, R2 (distributed in India and its neighbours) cannot be found in far east Siberia. Thus, P-M45 except some samples mentioned above virtually means Q-M242 (xM3). In the paper, 35.3% of Nivkhs and 20.8% of Chukchi people and 18.2% of Siberian Eskimos are shown in P-M45, and 12.5% of Chukchis and 21.2% of Siberian Eskimos are in Q-M3. All of them can be estimated to be in haplogroup Q.</ref> It is found in 30.8% of [[Yukaghir people|Yukaghirs]] who live in the basin of the [[Kolyma River]], which is located northwest of [[Kamchatka Peninsula|Kamchatka]].<ref name="Pakendorf2006"/> It is also found in 15% (Q1a* 9%, Q-M3 6%) of [[Koryaks]] in Kamchatka.<ref name = "Battaglia2013"/> |
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*'''Q''' M242 |
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**'''Q1''' P36.2, L232, L273, L274 |
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***'''Q1a''' MEH2 |
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****'''Q1a1''' M120, M265/N14 |
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****'''Q1a2''' M25, M143 |
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****[[Haplogroup Q1a3 (Y-DNA)|'''Q1a3''']] L56, L57, M346, L528 |
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***** '''Q1a3a''' L53, L54, L55, L213, L331 |
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******[[Haplogroup Q1a3a (Y-DNA)|'''Q1a3a1''']] M3 |
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*******'''Q1a3a1a''' M19 |
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*******'''Q1a3a1b''' M194 |
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*******'''Q1a3a1c''' M199, P106, P292 |
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******'''Q1a3a2''' L191 |
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******'''Q1a3a3''' L330, L334 |
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*******'''Q1a3a3a''' L329, L332, L333 |
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*****'''Q1a3b''' M323 |
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*****'''Q1a3c''' L527, L529 |
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***'''Q1b''' L275, L314 |
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****'''Q1b1''' M378/Page100, L214, L215/Page82 |
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*****'''Q1b1a''' L245 |
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******'''Q1b1a1''' L272.1 |
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== |
====East Asia==== |
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In some studies, various subgroups of Q-M242 are observed in [[Mongolia]]. Q1a2-M346 (mostly Q-L330) occupies 1.4<ref name=Battaglia2013/>~3.1%<ref name=Cristofaro2013/> of [[Mongols]] (1/2~2/3 among Q samples), followed by Q1a1a1-M120 (0.25<ref name=Battaglia2013/>~1.25%<ref name=Cristofaro2013/>), Q1a1b-M25 (0.25<ref name=Battaglia2013/>~0.63%<ref name=Cristofaro2013/>), Q1b-M378. In another study, Q is found in 4% of Mongols.<ref name=Bortolini2003/> Karafet ''et al.'' (2018) found Q-L54(xM3) in 2.7% (2/75) and Q-M25 in another 2.7% (2/75) for a total of 5.3% (4/75) haplogroup Q Y-DNA in a sample of Khalkha Mongols from Ulaanbaatar, Mongolia.<ref name = "Karafet2018">{{cite journal|last1=Karafet|first1=Tatiana M.|last2=Osipova|first2=Ludmila P.|last3=Savina|first3=Olga V.|display-authors=etal|year=2018|title=Siberian genetic diversity reveals complex origins of the Samoyedic-speaking populations|journal=American Journal of Human Biology|volume=30|issue=6|page=e23194|doi=10.1002/ajhb.23194|pmid=30408262|doi-access=free}}</ref> Based on these studies, the average frequency of Q-M242 in Mongols is estimated to be about 4~5%. |
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Haplogroup Q may be one of the most widely distributed Y-chromosome lineages in the modern world. It is found in [[Americas|the Americas]], [[North Africa]], [[East Asia]], [[South Asia]], [[West Asia]], and in [[Europe]]. |
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However, most of Q-M242 people in [[East Asia]] belong to subclade Q-M120, which distributes most intensively across northern China (the provinces of which the capitals locate northern to [[Huai River]]-[[Qin Mountains]] line). Q-M242 ranged from 4~8% in [[northwest China]] ([[Xinjiang]], [[Gansu]], [[Shaanxi]]), [[north China]] ([[Shanxi]], [[Hebei]]), [[central China]] ([[Henan]]), and upper [[east China]] ([[Shandong]]) to 3~4% in [[northeast China]]. The average frequency of Q-M242 in northern China is around 4.5%. However, it decreases to about 2% in southern China.<ref name=BoWen2004/><ref name="BingSuHimalaya"/> In a study published in 2011, researchers have found Q-M242 in 3.3% (12/361) of the samples of unrelated Han-Chinese male volunteers at Fudan University in Shanghai with the origins from all over China, though with the majority coming from east China.<ref name = "Yan2011">{{cite journal|last1=Yan|first1=Shi|last2=Chuan-|last3=Wang|first3=Chao|last4=Li|first4=Hui|display-authors=etal|year=2011|title=An updated tree of Y-chromosome Haplogroup O and revised phylogenetic positions of mutations P164 and PK4|journal=European Journal of Human Genetics|volume=19|issue=9|pages=1013–1015|doi=10.1038/ejhg.2011.64|pmid=21505448|pmc=3179364}}</ref> In another study published in 2011, Hua Zhong ''et al.'' found haplogroup Q-M242 in 3.99% (34/853, including 30/853 Q-M120, 3/853 Q-M346, and 1/853 Q-M25) of a pool of samples of Han Chinese from northern China and 1.71% (15/876, including 14/876 Q-M120 and 1/876 Q-M346) of a pool of samples of Han Chinese from southern China.<ref name = "Zhong2011">{{cite journal|last1=Zhong|first1=Hua|last2=Shi|first2=Hong|last3=Qi|first3=Xue-Bin|last4=Duan|first4=Zi-Yuan|last5=Tan|first5=Ping-Ping|last6=Jin|first6=Li|last7=Su|first7=Bing|last8=Ma|first8=Runlin Z.|year=2011|title=Extended Y Chromosome Investigation Suggests Postglacial Migrations of Modern Humans into East Asia via the Northern Route|journal=Mol. Biol. Evol.|volume=28|issue=1|pages=717–727|doi=10.1093/molbev/msq247|pmid=20837606|doi-access=free}}</ref> Q1a1-M120 is unique to East Asians. It is not found in South east Asia except with low diversity in Y-STR among southern Han Chinese indicating it spread during the Neolithic with Han Chinese culture to southern China from northern China. Q1a3*-M346 is only found among Hui and southern Han Chinese in South East Asia in southern China but not found in non-Han indigenous peoples at all. It came from northern China (north east Asia) with the Han. Only Native Americans have Q1a3a-M3, which is a descendant haplogroup of Q1a3*-M346. The Americas was populated by migrants from Central Asia in prehistoric times.<ref>{{cite journal|last1=Zhong|first1=Hua|last2=Shi|first2=Hong|last3=Qi|first3=Xue-Bin|last4=Duan|first4=Zi-Yuan|last5=Tan|first5=Ping-Ping|last6=Jin|first6=Li|last7=Su|first7=Bing|last8=Ma|first8=Runlin Z.|date=2011|title=Extended Y Chromosome Investigation Suggests Postglacial Migrations of Modern Humans into East Asia via the Northern Route|url=http://mbe.oxfordjournals.org/content/28/1/717.full.pdf|archive-url=https://web.archive.org/web/20200507003801/https://webcache.googleusercontent.com/search?q=cache:http://mbe.oxfordjournals.org/content/28/1/717.full.pdf%2Bhtml|url-status=live|archive-date=2020-05-07|journal=Mol. Biol. Evol.|volume=28|issue=1|pages=717–727|doi=10.1093/molbev/msq247|publisher=Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution|pmid=20837606|doi-access=free}}</ref> Q1a1 is attested in over 3,000 year old Han Chinese ancestral remains in the Shang and Zhou dynasties from the Hengbei archeological site.<ref>{{cite journal|last1=Zhao|first1=Yong-Bin|last2=Zhang|first2=Ye|last3=Li|first3=Hong-Jie|last4=Cui|first4=Ying-Qiu|last5=Zhu|first5=Hong|last6=Zhou|first6=Hui|date=Nov–Dec 2014|title=Ancient DNA evidence reveals that the Y chromosome haplogroup Q1a1 admixed into the Han Chinese 3,000 years ago|url=https://www.ncbi.nlm.nih.gov/pubmed/25130911|journal=Am J Hum Biol|volume=26|issue=6|pages=813–21|doi=10.1002/ajhb.22604|pmid=25130911|s2cid=20553478}}</ref> Modern northern Han Chinese Y haplogroups and mtdna match those of ancient northern Han Chinese ancestors 3,000 years ago from the Hengbei archeological site. 89 ancient samples were taken. Y haplogroups O3a, O3a3, M, O2a, Q1a1, and O* were all found in Hengbei samples.<ref>{{cite journal|first1=Yong-Bin|last1=Zhao|first2=Ye|last2=Zhang|first3=Quan-Chao|last3=Zhang|first4=Hong-Jie|last4=Li|first5=Ying-Qiu|last5=Cui|first6=Zhi|last6=Xu|first7=Li|last7=Jin|first8=Hui|last8=Zhou|first9=Hong|last9=Zhu|date=May 4, 2015|title=Ancient DNA Reveals That the Genetic Structure of the Northern Han Chinese Was Shaped Prior to 3,000 Years Ago|journal=PLOS One|volume=10|issue=5|pages=e0125676|doi=10.1371/journal.pone.0125676|pmid=25938511|pmc=4418768|bibcode=2015PLoSO..1025676Z|doi-access=free}}</ref> |
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===The Americas=== |
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{{Further|Indigenous Amerindian genetics|Y-DNA haplogroups in Indigenous peoples of the Americas}} |
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Q-M242 has been found with notable frequency in some samples of [[Uyghur people|Uyghurs]]: 15.38% (22/143, including 6/143 Q-M378, 5/143 Q-P36.2*, 4/143 Q-M120, 4/143 Q-M346, 1/143 Q-M25) of a sample of Uyghurs from the Turpan area (吐鲁番地区),<ref name = "Lu2011">Lu Yan (2011), "Genetic Mixture of Populations in Western China." Shanghai: Fudan University, 2011: 1-84. (Doctoral dissertation in Chinese: 陆艳, "中国西部人群的遗传混合", 上海:复旦大学,2011: 1-84.)</ref> 7.9% (6/76, including 2/76 Q1b1-L215/Page82/S325, 1/76 Q1a2-M346*, 1/76 Q1a1a1-M120, 1/76 Q1a2a1c-L330*, 1/76 Q1a2a1c1-L332) of a sample of Dolan Uyghurs (刀郎人) from Horiqol Township of Awat County,<ref name = "Liu2018" /> and 7.74% (37/478, including 24/478 Q-M346, 7/478 Q-P36.2*, 5/478 Q-M120) of a sample of Uyghurs from the Hotan area (和田地区).<ref name="Shan2014">{{cite journal|last1=Shan|display-authors=etal|date=Sep 2014|title=Genetic polymorphism of 17 Y chromosomal STRs in Kazakh and Uighur populations from Xinjiang, China|journal=Int J Legal Med|volume=128|issue=5|pages=743–4|doi=10.1007/s00414-013-0948-y|pmid=24398978|s2cid=23248209}}</ref> However, other studies have found haplogroup Q in much smaller percentages of Uyghur samples: 3.0% (2/67) Q-P36 Uygur,<ref name = "Hammer2006" /> 1.6% (1/64) Q-M120 Lop Uyghur (罗布人).<ref name = "Liu2018">{{cite journal|last1=LIU|first1=Shuhu|last2=NIZAM|first2=Yilihamu|last3=RABIYAMU|first3=Bake|last4=ABDUKERAM|first4=Bupatima|last5=DOLKUN|first5=Matyusup|title=应用Y染色体SNP对新疆三个隔离人群遗传多样性的研究 – 中国知网|trans-title=A study of genetic diversity of three isolated populations in Xinjiang using Y-SNP|language=Chinese|journal=Acta Anthropologica Sinica|date=February 2018|volume=37|issue=1|pages=146–156|doi=10.16359/j.cnki.cn11-1963/q.2017.0067}}</ref> Haplogroup Q was not observed in a sample of 39 Keriyan Uyghurs (克里雅人) from the village of Darya Boyi, located on the Keriya River deep in the Taklamakan Desert.<ref name = "Liu2018" /> |
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Haplogroup Q is the predominant Y-chromosome haplogroup in [[indigenous peoples of the Americas]]. |
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Haplogroup Q was observed in 3.2% (5/156 : 2 Q-M120, 3 Q-M346) of males in [[Tibet]] in one study<ref name=Gayden2007/> and in 1.23% (29/2354) of males in Tibet in another study,<ref name = "Qi2013">{{cite journal|last1=Qi|first1=Xuebin|last2=Cui|first2=Chaoying|last3=Peng|first3=Yi|display-authors=etal|year=2013|title=Genetic Evidence of Paleolithic Colonization and Neolithic Expansion of Modern Humans on the Tibetan Plateau|journal=Mol. Biol. Evol.|volume=30|issue=8|pages=1761–1778|doi=10.1093/molbev/mst093|pmid=23682168|doi-access=free}}</ref> but this haplogroup was not observed in a sample of males from Tibet (''n''=105) in a third study.<ref name = "Hammer2006" /> |
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Approximately 20,000 to 15,000 years ago, a group migrated [[Models of migration to the New World|from Asia into the Americas]] by crossing the [[Bering Strait]].<ref name=Zegura/> Many of the men in this group must have belonged to haplogroup Q for it now accounts for the majority of non-European haplogroups in [[indigenous peoples of the Americas]]. |
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It is found in about 1.9% of South [[Koreans]],<ref name=Kim2010>{{cite journal|last1=Kim|first1=Soon-Hee|display-authors=etal|date=Nov 2010|title='Y chromosome homogeneity in the Korean population|journal=Int J Legal Med|volume=124|issue=6|pages=653–7|doi=10.1007/s00414-010-0501-1|pmid=20714743|s2cid=27125545}}</ref><ref>{{cite journal|last1=Jin Park|first1=Myung|display-authors=etal|year=2012|title=Understanding the Y chromosome variation in Korea-relevance of combined haplogroup and haplotype analyses|journal=International Journal of Legal Medicine|volume=126|issue=4|pages=589–599|doi=10.1007/s00414-012-0703-9|pmid=22569803|s2cid=27644576}}</ref><ref>The frequencies of Q-M242 shown in both studies (Kim2010, Park2012) are 1.4% (7/506, Kim) and 1.8% (13/706, Park) respectively. But, if recalculated by regional population weights, the adjusted frequencies reach 1.87% (Kim) and 1.91% (Park) respectively, converging to 1.9%.</ref> showing the highest frequency in [[Seoul]] and [[Gyeonggi Province]] at 2.7% and decreasing ones to the south (Kim 2010). It has been found in about 0.3% of [[Japanese people|Japanese]]<ref name = "Underhill2000">Peter A. Underhill, Peidong Shen, Alice A. Lin, ''et al''. (2000), "Y chromosome sequence variation and the history of human populations." ''Nature Genetics'', Volume 26, November 2000.</ref><ref name = "Hammer2006">{{cite journal|last1=Hammer|first1=Michael F.|last2=Karafet|first2=Tatiana M.|last3=Park|first3=Hwayong|display-authors=etal|year=2006|title=Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes|journal=Journal of Human Genetics|volume=51|issue=1|pages=47–58|doi=10.1007/s10038-005-0322-0|pmid=16328082|doi-access=free}}</ref><ref name = "Xue2006">{{cite journal|last1=Xue|first1=Yali|last2=Zerjal|first2=Tatiana|last3=Bao|first3=Weidong|last4=Zhu|first4=Suling|last5=Shu|first5=Qunfang|last6=Xu|first6=Jiujin|last7=Du|first7=Ruofu|last8=Fu|first8=Songbin|last9=Li|first9=Pu |last10=Hurles |first10=Matthew E.|last11=Yang|first11=Huanming|last12=Tyler-Smith|first12=Chris|title=Male Demography in East Asia: A North–South Contrast in Human Population Expansion Times|journal=Genetics|date=April 2006|volume=172|issue=4|pages=2431–2439|doi=10.1534/genetics.105.054270|pmid=16489223|pmc=1456369}}</ref><ref name=Nonaka2007/><ref name = "Poznik2016" /> (with known examples from [[Shizuoka Prefecture|Shizuoka]]<ref name = "Hammer2006" /> and [[Saitama Prefecture|Saitama]]<ref name = "Nonaka2007" />) and in 0.3%<ref name=Trejaut2014/>~1.2%<ref name=Wang2014/> of [[Taiwanese people|Taiwanese]]. |
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Indeed, haplogroup Q has been found in approximately 94% of [[Indigenous peoples of the americas|Indigenous]] peoples of [[South America]]<ref>{{cite journal |doi=10.1086/377588 |title=Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas |year=2003 |last1=Bortolini |first1=M |last2=Salzano |first2=F |last3=Thomas |first3=M |last4=Stuart |first4=S |last5=Nasanen |first5=S |last6=Bau |first6=C |last7=Hutz |first7=M |last8=Layrisse |first8=Z |last9=Petzlerler |first9=M |journal=The American Journal of Human Genetics |volume=73 |issue=3 |pages=524 |pmid=12900798 |pmc=1180678}}</ref> and detected in [[Na-Dene languages|Na-Dené speakers]] at a rate of 25-50%, and North American [[Eskimo–Aleut languages|Eskimo–Aleut]] populations at about 46%.<ref name=genetree>{{cite web|title=Frequency Distribution of Y-DNA Haplogroup Q M3|url=http://www.genetree.com/education/q|publisher=GeneTree |year=2010 |accessdate=2010-01-30}}</ref> |
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In more modern population groups from the Americas, all Q samples tested for M346 have been positive. This founding population spread throughout the Americas. In the Americas, a member of the founding population underwent a mutation, producing its descendant population defined by the M3 [[single nucleotide polymorphism]] (SNP).<ref name=Zegura/> Many members of haplogroup Q in the [[Americas]] belong to the Q-M3 subclade.<ref name="Genebase"/> |
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Subclade Q1b-M378 is also found in China and its neighboring countries at very low frequencies. It exists throughout all Mongolia, with rare examples in Japan.<ref>{{cite journal|last1=Yamamoto|first1=Toshimichi|last2=Senda|first2=Tomoki|last3=Horiba|first3=Daiki|last4=Sakuma|first4=Masayoshi|last5=Kawaguchi|first5=Yuuka|last6=Kano|first6=Yuuichi|title=Y-chromosome lineage in five regional Mongolian populations|journal=Forensic Science International: Genetics Supplement Series|date=2013|volume=4|issue=1|pages=e260–e261|doi=10.1016/j.fsigss.2013.10.133}}</ref> |
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However, a 4000-year-old [[Saqqaq culture|Saqqaq]] individual belonging to Q-MEH2 haplogroup has been documented.<ref>{{cite web|title=Ancient human genome sequence of an extinct Palaeo-Eskimo|url=http://www.nature.com/nature/journal/v463/n7282/full/nature08835.html |publisher=Nature Publishing Group|pages= 463, 757–762|year=2010 |doi=10.1038/nature08835 |accessdate=2010-02-11}}</ref> |
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===Asia=== |
====Southeast Asia==== |
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Haplogroup Q shows low frequencies in [[Southeast Asia]]. In a study,<ref name="Kim2011">{{cite journal|last1=Kim|first1=Soon-Hee|display-authors=etal|year=2011|title=High frequencies of Y-chromosome haplogroup O2b-SRY465 lineages in Korea: a genetic perspective on the peopling of Korea|journal=Investigative Genetics|volume=2|issue=1|page=10|doi=10.1186/2041-2223-2-10|pmid=21463511|pmc=3087676|doi-access=free}}</ref> the frequencies of haplogroup Q is 5.4% (2/37) in [[Indonesia]], 3.1% (2/64) in the [[Philippines]], 2.5% (1/40) in [[Thailand]]. However, other studies show 0% or near 0% frequencies in those countries.<ref name=Trejaut2014/> |
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In the case of [[Vietnam]], the frequency is 7.1% in one study of a sample of Vietnamese reported to be from southern Vietnam<ref name="Karafet2005">{{cite journal|last1=Karafet|first1=TM|display-authors=etal|date=Feb 2005|title=Balinese Y-chromosome perspective on the peopling of Indonesia: genetic contributions from pre-neolithic hunter-gatherers, Austronesian farmers, and Indian traders|journal=Hum. Biol.|volume=77|issue=1|pages=93–114|doi=10.1353/hub.2005.0030|pmid=16114819|hdl=1808/13586|s2cid=7953854|hdl-access=free}}</ref><ref name = "He2012">{{cite journal|last1=He|first1=J-D|last2=Peng|first2=M-S|last3=Quang|first3=HH|last4=Dang|first4=KP|last5=Trieu|first5=AV|display-authors=etal|year=2012|title=Patrilineal Perspective on the Austronesian Diffusion in Mainland Southeast Asia|journal=PLOS One|volume=7|issue=5|page=e36437|doi=10.1371/journal.pone.0036437|pmid=22586471|pmc=3346718|bibcode=2012PLoSO...736437H|doi-access=free}}</ref> and 4.3% in a sample of [[Vietnamese people|Kinh people]] from [[Ho Chi Minh City]] in southern Vietnam,<ref name = "Poznik2016">{{cite journal|last1=Poznik|first1=G. David|last2=Xue|first2=Yali|last3=Mendez|first3=Fernando L.|display-authors=etal|date=June 2016|title=Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences|journal=Nature Genetics|volume=48|issue=6|pages=593–599|doi=10.1038/ng.3559|pmid=27111036|pmc=4884158}}</ref> but 0% or under 1% in other studies in which samples have been collected in [[Hanoi]] in northern Vietnam.<ref name=Kim2011/><ref name = "He2012" /><ref name=Trejaut2014/> So, it is hard to define average frequencies. However, Macholdt ''et al.'' (2020) have tested a sample of fifty [[Vietnamese people|Kinh]] people from northern Vietnam (all but one of whom are from the [[Hong River Delta|Red River Delta]] region, and 42 of whom are from [[Hanoi]]) and found that two of them (4%) belong to Q-M120.<ref name = "Macholdt2020">Enrico Macholdt, Leonardo Arias, Nguyen Thuy Duong, ''et al''., "The paternal and maternal genetic history of Vietnamese populations." ''European Journal of Human Genetics'' (2020) 28:636–645. https://doi.org/10.1038/s41431-019-0557-4</ref> |
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Likely due to its origin in [[Central Asia]], haplogroup Q may be found throughout [[Asia]].<ref name=Zegura>{{cite journal |author=Zegura SL, Karafet TM, Zhivotovsky LA, Hammer MF |title=High-resolution SNPs and microsatellite haplotypes point to a single, recent entry of Native American Y-chromosomes into the Americas |journal=Mol. Biol. Evol. |volume=21 |issue=1 |pages=164–75 |year=2004 |month=January |pmid=14595095 |doi=10.1093/molbev/msh009 |url=http://mbe.oxfordjournals.org/cgi/reprint/21/1/164.pdf}}</ref> It has been reported that Q is found in the [[Altai people]],<ref name = "Kharkov2007" /> [[India]],<ref name="ycc">[http://ycc.biosci.arizona.edu/new_binary_polymorphism/resultsanddiscussions.html The Y Chromosome Consortium 2008]</ref> [[Tibet]],<ref name=Gayden2007/> [[Pakistan]],<ref name="ycc" /> [[China]],<ref name=BoWen2004/><ref name = "BingSuHimalaya">{{cite journal |doi=10.1007/s004390000406 |title=Y chromosome haplotypes reveal prehistorical migrations to the Himalayas |year=2000 |last1=Su |first1=Bing |last2=Xiao |first2=Chunjie |last3=Deka |first3=Ranjan |last4=Seielstad |first4=Mark T. |last5=Kangwanpong |first5=Daoroong |last6=Xiao |first6=Junhua |last7=Lu |first7=Daru |last8=Underhill |first8=Peter |last9=Cavalli-Sforza |first9=Luca |journal=Human Genetics |volume=107 |issue=6 |pages=582–90 |pmid=11153912}}</ref> [[Mongolia]],<ref name = "Hammer2005">{{cite journal |doi=10.1007/s10038-005-0322-0 |title=Dual origins of the Japanese: Common ground for hunter-gatherer and farmer Y chromosomes |year=2005 |last1=Hammer |first1=Michael F. |last2=Karafet |first2=Tatiana M. |last3=Park |first3=Hwayong |last4=Omoto |first4=Keiichi |last5=Harihara |first5=Shinji |last6=Stoneking |first6=Mark |last7=Horai |first7=Satoshi |journal=Journal of Human Genetics |volume=51 |pages=47–58 |pmid=16328082 |issue=1 }}</ref> [[Tuvans]],<ref name = "Pakendorf2006">{{cite journal | last1 = Pakendorf | first1 = Brigitte | last2 = Novgorodov | first2 = Innokentij N. | last3 = Osakovskij | first3 = Vladimir L. | author-separator =, | last4 = Danilova | author-name-separator= | first4 = Al’Bina P.| year = 2006 | last5 = Protod’Jakonov | first5 = Artur P. | last6 = Stoneking | first6 = Mark | title = Investigating the effects of prehistoric migrations in Siberia: genetic variation and the origins of Yakuts | url = | journal = Human Genetics | volume = 120 | issue = 3| pages = 334–353 | doi = 10.1007/s00439-006-0213-2 | pmid=16845541}}</ref> and [[Uyghur people|Uyghurs]].<ref name = "Hammer2005" /> It is found at a frequency of more than 50% in the Pasthuns in Kabul the Capital of Afghanistan [http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0034288] |
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Only some regions and ethnic groups in the continent show high frequencies. Q-M242 is found in 2.8% (3/106, all Q-M346) in [[Myanmar]], and all the Q samples are concentrated in 18.8% in [[Ayeyarwady Region|Ayeyarwady]] (2/11) and 7.1% [[Bago, Myanmar|Bago]] (1/14) regions in southwest Myanmar.<ref name="Peng2013">{{cite journal|last1=Peng|first1=Min-Sheng|display-authors=etal|date=Aug 2014|title=Retrieving Y chromosomal haplogroup trees using GWAS data|journal=Eur J Hum Genet|volume=22|issue=8|pages=1046–1050|doi=10.1038/ejhg.2013.272|pmid=24281365|pmc=4350590}}</ref> And, Q-M242 is found in 55.6% (15/27) in the [[Akha people|Akha]] tribe in northern [[Thailand]].<ref name=Trejaut2014>{{cite journal|last1=Trejaut|first1=J.A.|year=2014|title=Taiwan Y-chromosomal DNA variation and its relationship with Island Southeast Asia|journal=BMC Genetics|volume=15|page=77|doi=10.1186/1471-2156-15-77|pmid=24965575|pmc=4083334|doi-access=free}}</ref> |
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==== East Asia ==== |
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====Central Asia==== |
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To the east, haplogroup Q has been found in approximately 4% of [[Altai people|Southern Altaians]] and 32% of [[Altai people|Northern Altaians]].<ref name = "Kharkov2007">V. N. Kharkov, V. A. Stepanov, O. F. Medvedeva, M. G. Spiridonova, M. I. Voevoda, V. N. Tadinova, and V. P. Puzyrev, "Gene Pool Differences between Northern and Southern Altaians Inferred from the Data on Y-Chromosomal Haplogroups," ''Genetika'' (2007), Vol. 43, No. 5, pp. 675–687.</ref> It is found in 16% of [[Tuvans]].<ref name="Pakendorf2006"/> |
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In [[Central Asia]], the southern regions show higher frequencies of Q than the northern ones. |
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In the northern regions, Q-M242 is found in about 2%<ref>{{cite journal|last1=Turspekov|display-authors=etal|year=2012|title=The Kazakhstan DNA project hits first hundred Y-profiles for ethnic Kazakhs|journal=The Russian Journal of Genetic Genealogy|volume=2|page=1}}</ref>~6%<ref name=Wells2001/><ref name=Seielstad2003>{{cite journal|last1=Seielstad|first1=Mark|display-authors=etal|date=Sep 2003|title=A Novel Y-Chromosome Variant Puts an Upper Limit on the Timing of First Entry into the Americas|journal=The American Journal of Human Genetics|volume=73|issue=3|pages=700–705|doi=10.1086/377589|pmid=12929085|pmc=1180698}}</ref> (average 4%) of [[Kazakhs]]. A study published in 2017 found haplogroup Q Y-DNA in 3.17% (41/1294) of a large pool of samples of [[Kazakh tribes]]; however, haplogroup Q was concentrated in the members of the [[Qangly]] tribe (27/40 = 67.5%), and it was much less common among the other tribes.<ref name = "Ashirbekov2017">E. E. Ashirbekov, D. M. Botbaev, A. M. Belkozhaev, A. O. Abayldaev, A. S. Neupokoeva, J. E. Mukhataev, B. Alzhanuly, D. A. Sharafutdinova, D. D. Mukushkina, M. B. Rakhymgozhin, A. K. Khanseitova, S. A. Limborska, and N. A. Aytkhozhina, "Distribution of Y-Chromosome Haplogroups of the Kazakh from the South Kazakhstan, Zhambyl, and Almaty Regions." Reports of the National Academy of Sciences of the Republic of Kazakhstan, ISSN 2224-5227, Volume 6, Number 316 (2017), 85 – 95.</ref> The Qangly tribe is related at least in name to the earlier [[Kankalis]] and probably also the [[Kangar union]]. Haplogroup Q is found in about 2% of [[Kyrgyz people]].<ref name=Cristofaro2013/><ref name=Wells2001/><ref name=Seielstad2003/> |
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The frequency of Q in northern China is about 4%, with many Chinese samples of haplogroup Q belonging to the subclade Q-M120.<ref name=BoWen2004/><ref name="BingSuHimalaya"/> Haplogroup Q is found in approximately 3% of males in [[Tibet]]<ref name=Gayden2007/> and [[Mongolia]].<ref name="Hammer2005"/> |
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It is also found in 3% of [[Uyghur people|Uyghurs]].<ref name = "Hammer2005" /> |
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In the southern regions, Q-M242 is found in 5%<ref name=Malyarchuk2013>{{cite journal|last1=Malyarchuk|first1=B|display-authors=etal|date=Jan 2013|title=Y-chromosome variation in Tajiks and Iranians|journal=Ann. Hum. Biol.|volume=40|issue=1|pages=48–54|doi=10.3109/03014460.2012.747628|pmid=23198991|s2cid=2752490}}</ref>~6%<ref name=Wells2001/><ref name=Seielstad2003/> of [[Tajiks]] ([[Tajikistan]]). Karafet ''et al.'' 2001 found P-DYS257(xQ1b1a1a-M3, R-UTY2), which should be roughly equivalent to haplogroup Q-M242(xM3), in 4/54 = 7.4% of a sample of [[Uzbeks]], apparently sampled in Uzbekistan.<ref name=Karafet2001>{{cite journal|last1=Karafet|display-authors=etal|date=Sep 2001|title=Paternal Population History of East Asia: Sources, Patterns, and Microevolutionary Processes|journal=The American Journal of Human Genetics|volume=69|issue=3|pages=615–628|doi=10.1086/323299|pmid=11481588|pmc=1235490}}</ref> Wells ''et al.'' 2001 found P-M45(xM120, M124, M3, M173), which should be roughly equivalent to a mix of Q-M242(xM120, M3) and R2-M479(xR2a-M124), in 20/366 = 5.5% of a pool of samples of Uzbeks from seven different regions of Uzbekistan.<ref name = "Wells2001" /> Di Cristofaro ''et al.'' 2013 found Q-M242 in 11/127 = 8.7% of a pool of samples of Uzbeks from three different provinces of Afghanistan, including 5/94 Q-M242(xM120, M25, M346, M378), 4/94 Q-M346, and 1/94 Q-M25 (10/94 = 10.6% Q-M242 total) in a sample of Uzbeks from [[Jawzjan Province]], whose northern border abuts the southeastern corner of [[Turkmenistan]], and 1/28 Q-M242(xM120, M25, M346, M378) in a sample of Uzbeks from [[Sar-e Pol Province]].<ref name=Cristofaro2013/> Wells ''et al.'' (2001) found P-M45(xM120, M124, M3, M173) in 10.0% (3/30) of a sample of [[Turkmen people|Turkmens]] from [[Turkmenistan]], whereas Karafet ''et al.'' (2018) found Q-M25 in 50.0% (22/44) of another sample of Turkmens from Turkmenistan, so the frequency of haplogroup Q in that country is not yet clear. However, Grugni ''et al.'' (2012) found Q-M242 in 42.6% (29/68) of a sample of Turkmens from [[Golestan province|Golestan]], Iran, and Di Cristofaro ''et al.'' (2013) found Q-M25 in 31.1% (23/74) and Q-M346 in 2.7% (2/74) for a total of 33.8% (25/74) Q-M242 in a sample of Turkmens from [[Jawzjan Province|Jawzjan]], Afghanistan, so the frequency of Q-M242 may reach about 40% in [[Turkmens]] of [[Afghanistan]] and [[Iran]] who live in the areas adjacent to Turkmenistan. |
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The highest frequencies of Q in Asia are found among the [[Selkups]] (~70%) and [[Kets]] (~95%), they live in western and middle [[Siberia]] and their populations are small in number, being just under 5,000 and 1,500, respectively. |
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Q-M242 accounts for 6.9% of [[Citizen of Afghanistan|Afghans]] in a study (Haber 2012). In another study (Cristofaro 2013) with a larger sampling, the frequency of Q rises to 8.9% (45/507). Haplogroup Q occurs at a frequency of 8% (11/136) in Afghan [[Pashtuns]] and 3% (5/142) in Afghan [[Tajiks]].<ref>{{cite journal|last1=Haber|first1=Marc|last2=Platt|first2=Daniel E.|last3=Ashrafian Bonab|first3=Maziar|last4=Youhanna|first4=Sonia C.|last5=Soria-Hernanz|first5=David F.|last6=Martínez-Cruz|first6=Begoña|last7=Douaihy|first7=Bouchra|last8=Ghassibe-Sabbagh|first8=Michella|last9=Rafatpanah|first9=Hoshang |last10=Ghanbari |first10=Mohsen|last11=Whale|first11=John|last12=Balanovsky|first12=Oleg|last13=Wells|first13=R. Spencer|last14=Comas|first14=David|last15=Tyler-Smith|first15=Chris|last16=Zalloua|first16=Pierre A.|title=Afghanistan's Ethnic Groups Share a Y-Chromosomal Heritage Structured by Historical Events|journal=PLOS One|date=2012-03-28|volume=7|issue=3|pages=e34288|doi=10.1371/journal.pone.0034288|pmid=22470552|pmc=3314501|bibcode=2012PLoSO...734288H|doi-access=free}}</ref><ref>{{cite journal|last1=Di Cristofaro|first1=Julie|last2=Pennarun|first2=Erwan|last3=Mazières|first3=Stéphane|last4=Myres|first4=Natalie M.|last5=Lin|first5=Alice A.|last6=Temori|first6=Shah Aga|last7=Metspalu|first7=Mait|last8=Metspalu|first8=Ene|last9=Witzel|first9=Michael |last10=King |first10=Roy J.|last11=Underhill|first11=Peter A.|last12=Villems|first12=Richard|last13=Chiaroni|first13=Jacques|title=Afghan Hindu Kush: Where Eurasian Sub-Continent Gene Flows Converge|journal=PLOS One|date=2013-10-18|volume=8|issue=10|pages=e76748|doi=10.1371/journal.pone.0076748|pmid=24204668|pmc=3799995|bibcode=2013PLoSO...876748D|doi-access=free}}</ref> In this study(Cristofaro 2013), [[Turkmens]] of [[Jowzjan Province]] which is neighboring to [[Turkmenistan]] show the highest frequency at 33.8% (25/74: 23 Q-M25, 2 Q-M346), followed by [[Uzbeks]] at 8.7% (11/144: 6 Q*, 1 Q-M25, 4 Q-M346).<ref name=Cristofaro2013/> |
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==== South Asia ==== |
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====Southwest Asia==== |
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Some examples of Q* (negative for known subclades) have been reported in the [[Indian subcontinent]] in low frequency.<ref name=Sharma07>{{cite journal |author=Sharma S, Rai E, Bhat AK, Bhanwer AS, Bamezai RN |title=A novel subgroup Q5 of human Y-chromosomal haplogroup Q in India |journal=BMC Evol. Biol. |volume=7|pages=232 |year=2007 |pmid=18021436 |pmc=2258157 |doi=10.1186/1471-2148-7-232 }}</ref> The same studies have found Q-M346* (negative for known subclades) restricted to the Indian subcontinent. The most plausible explanation for these observations could be an ancestral migration of individuals bearing ancestral lineage Q* to the Indian subcontinent followed by an [[Indigenous peoples|autochthonous differentiation]] to Q-M346. However, these are from studies where all current branches of the Q tree have not been tested. |
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[[West Asia|Southwest Asia]] exhibits high frequencies of Q in northern [[Iran]], and gradually lowering ones to the southwest. |
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Q-M242 accounts for 5.5% (52/938) in Iran according to Grugni 2012, which shows a large and well allocated sampling. The Q samples (52) in the study consist of various subclades such as Q* (3), Q-M120 (1), Q-M25 (30), Q-M346 (8), Q-M378 (10). The highest frequency is at 42.6% (29/68, all Q-M25) in [[Turkmens]] of [[Golestan province|Golestan]], followed by 9.1% in [[Isfahan]] ([[Persian people]]), 6.8% in [[Khorasan province|Khorasan]] (Persian people), 6% in [[Lorestan province|Lorestan]] (Luristan, [[Persian people|Lurs]]), 4.9% in [[West Azerbaijan province|Azarbaijan Gharbi]] (5.1% of [[Assyrian people|Assyrians]] and 4.8% of [[Azerbaijanis|Azeris]]), 4.5% in [[Fars province|Fars]] (Persian people), and so on.<ref name=Grugni2012>{{cite journal|last1=Grugni|first1=Viola|display-authors=etal|year=2012|title=Ancient Migratory Events in the Middle East: New Clues from the Y-Chromosome Variation of Modern Iranians|journal=PLOS One|volume=7|issue=7|pages=e41252|doi=10.1371/journal.pone.0041252|pmid=22815981|pmc=3399854|bibcode=2012PLoSO...741252G|doi-access=free}}</ref> Turkmens are known as the descendants of [[Oghuz Turks]] who built many Turkic empires and dynasties. Other studies also show similar frequencies.<ref name=Regueiro2006>{{cite journal|last1=Regueiro|first1=M.|last2=Cadenas|first2=A.M.|last3=Gayden|first3=T.|last4=Underhill|first4=P.A.|last5=Herrera|first5=R.J.|title=Iran: Tricontinental Nexus for Y-Chromosome Driven Migration|journal=Human Heredity|date=2006|volume=61|issue=3|pages=132–143|doi=10.1159/000093774|pmid=16770078|s2cid=7017701}}</ref><ref name=Bekada2013>{{cite journal|last1=Bekada|first1=Asmahan|display-authors=etal|year=2013|title=Introducing the Algerian Mitochondrial DNA and Y-Chromosome Profiles into the North African Landscape|journal=PLOS One|volume=8|issue=2|page=e56775|doi=10.1371/journal.pone.0056775|pmid=23431392|pmc=3576335|bibcode=2013PLoSO...856775B|doi-access=free}}</ref><ref>The frequency of Q is 4% (6/150, all Q-M25) in Regueiro 2006, in which it is 9.1% (3/33) in north Iran and 2.6% (3/117) in south Iran. But, since more people live in the northern regions, if recalculated by population weights, the frequency will reach about 6%. It is also 6.2% (35/566) in Bekada 2013 with a large-scale sampling.</ref> |
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The problematic phylogeny sampling of early studies has been demonstrated by subsequent studies that have found Q-M346, Q-M378, and Q-M25 in South Asia. |
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In a study (Zahery 2011), the frequency of Q is 1.9% (3/154: all Q-M378) in [[Iraqis]] (x Marsh Arabs), and 2.8% (4/143: 1 Q-M25, 3 Q-M378) in [[Marsh Arabs]] who are known as the descendants of ancient [[Sumer]]ians.<ref name=Zahery2010>{{cite journal|last1=Al-Zahery|first1=Nadia|display-authors=etal|year=2011|title=In search of the genetic footprints of Sumerians: a survey of Y-chromosome and mtDNA variation in the Marsh Arabs of Iraq|journal=BMC Evolutionary Biology|volume=11|issue=1|page=288|doi=10.1186/1471-2148-11-288|pmid=21970613|pmc=3215667|bibcode=2011BMCEE..11..288A|doi-access=free}}</ref> |
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==== West Asia ==== |
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Two studies conducted Ivan Nasidze in 2004 and 2009, show that the frequency of Q in Iran, varies between approximately 2% to 6%, depending on region. Iranian samples of haplogroup Q belong primarily to the subclade Q-M25.<ref name=Regueiro2006>{{cite journal |author=Regueiro M, Cadenas AM, Gayden T, Underhill PA, Herrera RJ |title=Iran: tricontinental nexus for Y-chromosome driven migration |journal=Hum. Hered. |volume=61 |issue=3 |pages=132–43 |year=2006 |pmid=16770078 |doi=10.1159/000093774 }}</ref> |
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In [[Pakistan]], at the eastern end of the Iranian plateau, the frequency of haplogroup Q is about 2.2% (14/638)<ref name = "Firasat2007">{{cite journal | doi = 10.1038/sj.ejhg.5201726 | last1 = Firasat | first1 = Sadaf | last2 = Khaliq | first2 = Shagufta | last3 = Mohyuddin | first3 = Aisha | last4 = Papaioannou | first4 = Myrto | last5 = Tyler-Smith | first5 = Chris | last6 = Underhill | first6 = Peter A | last7 = Ayub | first7 = Qasim | year = 2007 | title = Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan | url = | journal = European Journal of Human Genetics | volume = 15 | issue = 1| pages = 121–126 | pmid = 17047675 | pmc = 2588664 }}</ref> or 3.4% (6/176).<ref name = "Sengupta2006" /> |
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Approximately 2.5% of males in [[Saudi Arabia]] belong to haplogroup Q.<ref name = "AbuAmero2009">{{cite journal |
Approximately 2.5% (4/157: 3 Q*, 1 Q-M346) of males in [[Saudi Arabia]] belong to haplogroup Q. It also accounts for 1.8% (3/164: 2 Q*, 1 Q-M346) in the [[United Arab Emirates]] and 0.8% (1/121: Q*) in [[Oman]] peoples.<ref name=Cadenas2008>{{cite journal|vauthors=Cadenas AM, Zhivotovsky LA, Cavalli-Sforza LL, Underhill PA, Herrera RJ|title=Y-chromosome diversity characterizes the Gulf of Oman|journal=Eur. J. Hum. Genet.|volume=16|issue=3|pages=374–86|date=March 2008|pmid=17928816|doi=10.1038/sj.ejhg.5201934|doi-access=free}}</ref><ref name="AbuAmero2009">{{cite journal|last1=Abu-Amero|first1=Khaled K.|last2=Hellani|first2=Ali|last3=Gonzalez|first3=Ana M.|last4=Larruga|first4=Jose M|year=2009|last5=Cabrera|first5=Vicente M|last6=Underhill|first6=Peter A|title=Saudi Arabian Y-Chromosome diversity and its relationship with nearby regions|journal=BMC Genetics|volume=10|issue=1|page=59|doi=10.1186/1471-2156-10-59|pmc=2759955|pmid=19772609|doi-access=free}}</ref> |
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Haplogroup Q-M242 has also been found in 1.1% (1/87, Q-P36) [[Syrian people|Syrians]]<ref name=Karafet2005/> and 2.0% (18/914, 14 Q*, 4 Q-M25) in [[Lebanese people|Lebanese]].<ref name=Zalloua2008>{{cite journal|vauthors=Zalloua PA, Xue Y, Khalife J|display-authors=etal|title=Y-Chromosomal Diversity in Lebanon Is Structured by Recent Historical Events|journal=Am. J. Hum. Genet.|volume=82|issue=4|pages=873–82|date=April 2008|pmid=18374297|pmc=2427286|doi=10.1016/j.ajhg.2008.01.020}}</ref> |
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According to Behar et al. 5% of Ashkenazi males belong to haplogroup Q.<ref name="behar">http://www.springerlink.com/content/xvj2jwclptvrvmer/</ref> This has subsequently been found to be entirely the Q-M378 subclade and may be restricted to Q-L245. |
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Approximately 2% (10/523: 9 Q*, 1 Q-M25) of males in [[Turkey]] belong to haplogroup Q.<ref name=Cinnioglu2004>{{cite journal|vauthors=Cinnioğlu C, King R, Kivisild T|display-authors=etal|title=Excavating Y-chromosome haplotype strata in Anatolia|journal=Hum. Genet.|volume=114|issue=2|pages=127–48|date=January 2004|pmid=14586639|doi=10.1007/s00439-003-1031-4|s2cid=10763736}}</ref> In a study (Gokcumen 2008), it was found that among [[Turkish people|Turks]] who belong to the [[Afshar people|Afshar tribe]] (one of [[Oghuz Turks]]) haplogroup Q-M242 is seen with a prevalence of 13%.<ref name="GoogleBooks-95573">{{cite book|url=https://books.google.com/books?id=V5oPGbeBnxkC|title=Ethnohistorical and Genetic Survey of Four Central Anatolian Settlements|isbn=978-0-549-80966-1|publisher=University of Pennsylvania|access-date=May 13, 2014|year=2008|first=Omer|last=Gokcumen}}</ref> |
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Haplogroup Q has also been found in [[Algeria]]ns, [[Arabia]]ns, [[Syrians]], [[Lebanese people|Lebanese]]<ref name=Zalloua2008>{{cite journal |author=Zalloua PA, Xue Y, Khalife J, ''et al'' |title=Y-Chromosomal Diversity in Lebanon Is Structured by Recent Historical Events |journal=Am. J. Hum. Genet. |volume=82 |issue=4 |pages=873–82 |year=2008 |month=April |pmid=18374297 |pmc=2427286 |doi=10.1016/j.ajhg.2008.01.020 }}</ref> and the [[United Arab Emirates]].,<ref name=Cadenas2008>{{cite journal |author=Cadenas AM, Zhivotovsky LA, Cavalli-Sforza LL, Underhill PA, Herrera RJ |title=Y-chromosome diversity characterizes the Gulf of Oman |journal=Eur. J. Hum. Genet. |volume=16 |issue=3 |pages=374–86 |year=2008 |month=March |pmid=17928816 |doi=10.1038/sj.ejhg.5201934 }}</ref> |
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====South Asia==== |
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Approximately 2% of males in [[Turkey]],<ref name=Cinnioglu2004>{{cite journal |author=Cinnioğlu C, King R, Kivisild T, ''et al'' |title=Excavating Y-chromosome haplotype strata in Anatolia |journal=Hum. Genet. |volume=114 |issue=2 |pages=127–48 |year=2004 |month=January |pmid=14586639 |doi=10.1007/s00439-003-1031-4 }}</ref> In a study by Gokcumen it was found that among [[Turkish people|Turks]] that belong to the [[Afshar tribe]] haplogroup Q is seen with a prevalence of 13%.<ref>{{cite journal |isbn=978-0-549-80966-1 }}</ref> Further, the Q-M25 subclade has been found in [[Turkey]]<ref name="Cinnioglu2004" /> |
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In [[Pakistan]] at the eastern end of the [[Iranian Plateau]], the frequency of haplogroup Q-M242 is about 2.2% (14/638)<ref name="Firasat2007">{{cite journal|doi=10.1038/sj.ejhg.5201726|last1=Firasat|first1=Sadaf|last2=Khaliq|first2=Shagufta|last3=Mohyuddin|first3=Aisha|last4=Papaioannou|first4=Myrto|last5=Tyler-Smith|first5=Chris|last6=Underhill|first6=Peter A|last7=Ayub|first7=Qasim|year=2007|title=Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan|journal=European Journal of Human Genetics|volume=15|issue=1|pages=121–126|pmid=17047675|pmc=2588664}}</ref>~3.4% (6/176).<ref name="Sengupta2006"/> |
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Q-M346 is found among the [[Khanty people|Khanty]].<ref name=Mirabal2009>{{cite journal |author=Mirabal S, Regueiro M, Cadenas AM, ''et al'' |title=Y-Chromosome distribution within the geo-linguistic landscape of northwestern Russia |journal=Eur. J. Hum. Genet. |volume= 17|issue= 10|pages= 1260–73|year=2009 |month=March |pmid=19259129 |pmc=2986641 |doi=10.1038/ejhg.2009.6 }}</ref> |
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In a study (Sharma2007), Q-M242 is observed in 2.38% (15/630) of [[Indian people]] belonging to different regions and social categories. What is interesting is 14/15 samples do not belong to any known subgroups of Q-M242, with 4 among them showing novel (Indian-specific) 'ss4bp' allele under Q-MEH2. This study also reflects the results of some former studies (Sengupta 2006, Seielstad 2003). And, the accumulated result (frequency) of 3 studies is turned out to be 1.3% (21/1615), with 11 out of 21 Q samples.<ref name=Sharma2007/> (For more information, see [[Y-DNA haplogroups in populations of South Asia]]) |
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In a regional study in [[Gujarat]] ([[Western India]]), Q-M242 was found at its highest 12% (3/25) among Nana Chaudharis while the overall percentage in Gujarat was found to be 2.8% (8/284).<ref>{{cite journal|last1=Khurana|first1=P|display-authors=etal|year=2014|title=Y Chromosome Haplogroup Distribution in Indo-European Speaking Tribes of Gujarat, Western India|journal=PLOS One|volume=9|issue=3|pages=e90414|doi=10.1371/journal.pone.0090414|pmid=24614885|pmc=3948632|bibcode=2014PLoSO...990414K|doi-access=free}}</ref> In another study, 2.6% of Tharus in Chitwan district and 6.1% (3/49) of Hindus in [[New Delhi]], the capital of India were found to be Q-M242 positive.<ref name=Fornarino2009>{{cite journal|last1=Fornarino|first1=Simona|display-authors=etal|year=2009|title=Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation|journal=BMC Evol. Biol.|volume=9|issue=1|page=154|doi=10.1186/1471-2148-9-154|pmid=19573232|pmc=2720951|bibcode=2009BMCEE...9..154F|doi-access=free}}</ref> |
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In a study in which Q-M242 is just classified in P* group, P* (x R1, R2) accounts for 9.7% (23/237: [[Chakma people|Chakma]] 13/89, [[Marma people|Marma]] 4/60, [[Tripura]] 6/88) in three ethnic groups of [[Bangladesh]].<ref>{{cite journal|last1=Nahar Gazi|first1=Nurun|display-authors=etal|year=2013|title=Genetic Structure of Tibeto-Burman Populations of Bangladesh: Evaluating the Gene Flow along the Sides of Bay-of-Bengal|journal=PLOS One|volume=8|issue=10|pages=e75064|doi=10.1371/journal.pone.0075064|pmid=24130682|pmc=3794028|bibcode=2013PLoSO...875064G|doi-access=free}}</ref> In many cases, all or most of P* (x R1, R2) means Q-M242, and thus most of P* (9.7%) samples in that study can be estimated to be Q-M242. |
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1.2% of [[Nepalese people]] in [[Kathmandu]], the capital of [[Nepal]] and 3.2% of people from [[Tibet]] are in Q-M242.<ref name=Gayden2007/> |
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3.3% of [[Demographics of Sri Lanka|Sri Lankans]]<ref name=Karafet2005/> are also in Q-M242. |
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===Europe=== |
===Europe=== |
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Q-M242 is distributed across most European countries at low frequencies, and the frequencies decrease to the west and to the south. |
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The frequency of haplogroup Q in [[Norway]] and [[Sweden]] is about 3%, while 2.5% of [[Slovak people|Slovak]] males are in haplogroup Q. |
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=== |
====Central- and Eastern Europe==== |
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{|class="wikitable" |
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In Central- [[Eastern Europe]], Q-M242 comprises about 1.7% of males. Q-M242 is found in about 2% of [[Russians]],<ref name=Malyarchuk2008>{{cite journal|last1=Malyarchuk|first1=B. A.|display-authors=etal|year=2008|title=Gene Pool Structure of Russian Populations from the European Part of Russia Inferred from the Data on Y Chromosome Haplogroups Distribution|journal=Russian Journal of Genetics|volume=44|issue=2|pages=187–192|doi=10.1134/S1022795408020105|s2cid=28165493}}</ref> 1.5% of [[Belarusians]],<ref name=Kharkov2005>{{cite journal|last1=Khar'kov|first1=VN|display-authors=etal|date=Aug 2005|title=Frequencies of Y chromosome binary haplogroups in Belarussians|journal=Genetika|volume=41|issue=8|pages=1132–6|pmid=16161635|doi=10.1007/s11177-005-0182-x|s2cid=1357824}}</ref> 1.3% of [[Ukrainians]]{{citation needed|date=April 2020}} 1.3% of [[Polish people|Poles]] (Poland),<ref>{{cite web|url=https://www.familytreedna.com/groups/polish/dna-results|title=Family Tree DNA – Genetic Testing for Ancestry, Family History & Genealogy}}</ref> 2% of [[Czechs]],<ref name=Ehler2011>{{cite journal|last1=Ehler|first1=Edvard|display-authors=etal|date=Jun 2011|title=Y-chromosomal diversity of the Valachs from the Czech Republic: model for isolated population in Central Europe|journal=Croat Med J|volume=52|issue=3|pages=358–367|doi=10.3325/cmj.2011.52.358|pmid=21674832|pmc=3131682}}</ref> 1.5% of [[Slovaks]],<ref>{{cite web|url=https://www.familytreedna.com/groups/slovakia/dna-results|title=Family Tree DNA – Genetic Testing for Ancestry, Family History & Genealogy}}</ref> about 2.2% of [[Hungarians]],{citation needed} 1.2% of [[Romanians]],<ref>{{cite web|url=https://www.familytreedna.com/groups/romania/dna-results|title=Family Tree DNA – Genetic Testing for Ancestry, Family History & Genealogy}}</ref> 0.8% of [[Moldovans]],<ref>{{cite journal|last1=Varzari|first1=Alexander|display-authors=etal|year=2013|title=Paleo-Balkan and Slavic Contributions to the Genetic Pool of Moldavians: Insights from the Y Chromosome|journal=PLOS One|volume=8|issue=1|pages=e53731|doi=10.1371/journal.pone.0053731|pmid=23341985|pmc=3547065|bibcode=2013PLoSO...853731V|doi-access=free}}</ref> and 0.5% (4/808: 2 Q-M378, 1 Q-M346, 1 Q-M25) of [[Bulgarians]]<ref name=Karachanak2013>{{cite journal|last1=Karachanak|first1=Sena|display-authors=etal|year=2013|title=Y-Chromosome Diversity in Modern Bulgarians: New Clues about Their Ancestry|journal=PLOS One|volume=8|issue=3|page=e56779|doi=10.1371/journal.pone.0056779|pmid=23483890|pmc=3590186|bibcode=2013PLoSO...856779K|doi-access=free}}</ref> On the other hand, 3.1% of [[Székelys]] from [[Transylvania]] (who have claimed to be descendants of [[Attila]]'s [[Huns]]) turned out to be P* (xR1-M173),<ref name=Csanyi2008>{{cite journal|last1=Csányi|first1=B.|display-authors=etal|title=Y-Chromosome Analysis of Ancient Hungarian and Two Modern Hungarian-Speaking Populations from the Carpathian Basin|journal=Annals of Human Genetics|volume=72|issue=4|pages=519–534|doi=10.1111/j.1469-1809.2008.00440.x|pmid=18373723|date=July 2008|s2cid=13217908}}</ref> which virtually means Q-M242. In a related DNA Project of FT-DNA, the frequency of Q-M25 in Székelys (Szeklers) reaches 4.3%.<ref>[https://www.familytreedna.com/groups/hungarian-bukovina-surnames/about/background Hungarian Bukovina]</ref><ref name="familytreedna.com">[https://www.familytreedna.com/groups/ydna-q-l-712/about/background Q-L712 Subclades of haplogroup Q-M25: Q-L712, Q-L715, Q-L713, Q-YP789]</ref> |
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! Population||||Paper||N||Percentage||SNPs Tested |
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The [[Caucasus]] region shows a frequency at 1.2% in a study,<ref name=Bekada2013/> but it may reach over 4% in [[Azerbaijan]], in that 4.9% of the neighboring [[Iranian Azerbaijanis]] harbor Q-M242.<ref name=Regueiro2006/> It is 1.3% in [[Georgians]] and [[Armenians]] respectively, and Armenian subclades consist of Q-M378 (L245), Q-M346, and Q-M25.<ref>{{cite web|url=https://www.familytreedna.com/groups/armeniadnaproject/dna-results|title=Family Tree DNA – Genetic Testing for Ancestry, Family History & Genealogy}}</ref> |
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| Austro-Asiatic (Khasi-Khmuic)||||Reddy 2009||353||5.40||P-M45(xM173) § |
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====Northern Europe==== |
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| Austro-Asiatic (Mundari)||||Reddy 2009||64||10.90||P-M45(xM173) § |
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| Nicobarese (Mon-Khmer)||||Reddy 2009||11||0.00||P-M45(xM173) § |
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| Austro-Asiatic (Southeast Asia)||||Reddy 2009||257||1.60||P-M45(xM173) § |
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| Garo (Tibeto-Burman)||||Reddy 2009||71||1.40||P-M45(xM173) § |
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| Tibeto-Burman (India)||||Reddy 2009||226||3.10||P-M45(xM173) § |
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| Tibeto-Burman (East Asia)||||Reddy 2009||214||0.00||P-M45(xM173) § |
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| Indo-European (Eastern India)||||Reddy 2009||54||18.50||P-M45(xM173) § |
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| Southern Talysh||Iran||Nasidze 2009||50||4.00||P-M45(xM124,xM173) |
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| Northern Talysh||Azerbaijan||Nasidze 2009||40||5.00||P-M45(xM124,xM173) |
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| Mazandarana||Iran||Nasidze 2009||50||4.00||P-M45(xM124,xM173) |
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| Gilakia||Iran||Nasidze 2009||50||0.00||P-M45(xM124,xM173) |
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| Iranians (Tehran)||Iran||Nasidze 2004||80||4.00||P-M45(xM124,xM173) |
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| Iranians (Isfahan)||Iran||Nasidze 2004||50||6.00||P-M45(xM124,xM173) |
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| Bakhtiari||Iran||Nasidze 2008||53||2.00||P-M45(xM124,xM173) |
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| Iranian Arabs||Iran||Nasidze 2008||47||2.00||P-M45(xM124,xM173) |
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| North Iran||Iran||Regueiro 2006||33||9.00||P-M45(xM124,xM173) |
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| South Iran||Iran||Regueiro 2006||117||3.00||P-M45(xM124,xM173) |
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| Georgians||South Caucacus||Nasidze and Stoneking 2001||77||3.00||P-M45(xM124,xM173) |
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| Armenians||South Caucacus||Nasidze and Stoneking 2001||100||2.00||P-M45(xM124,xM173) |
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| Azerbaijanis||South Caucacus||Nasidze and Stoneking 2001||72||0.00||P-M45(xM124,xM173) |
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§ ''These may include members of haplogroup [[Haplogroup R2 (Y-DNA)|R2]].'' |
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In [[Northern Europe]], haplogroup Q comprises about 2.5% of males. According to the Swedish Haplogroup Database, 4.1% (27/664, as of Jan 2016) of [[Swedes|Swedish]] males belong to Q-M242. About 2/3 of the samples analyzed subclades in detail belong to Q1a2b-F1161/L527 and about 1/3 are in Q1a2a-L804. By county, they are distributed intensively in the southern region ([[Götaland]],: not to be confused with [[Gotland]]), and rarely to the north. If recalculated by county-population weights, the frequency of Q in Sweden reaches 4.7%. |
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===Subclade Distribution=== |
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In [[Norway]], Q-M242 is found in about 2.6% (~4%<ref name=Faux2007/>) of males, with Q-L804 being more common than Q-F1161/L527.<ref>{{cite web|url=https://www.familytreedna.com/groups/norway/dna-results|title=Family Tree DNA – Genetic Testing for Ancestry, Family History & Genealogy}}</ref> It is observed among 1.6% of males in [[Denmark]], 3% in the [[Faroe Islands]] (known to be related to [[Vikings]]).<ref>Allison Mann, Vikings, merchants, and pirates at the top of the world : Y-chromosomal signatures of recent and ancient migrations in the Faroe Islands, MA Thesis of University of Louisville, 2012.</ref> In an article (Helgason et al.) on the haplotypes of [[Icelanders]], 7.2% (13/181) of males in [[Iceland]] are labelled as R1b-Branch A, but they are actually Q-M242.<ref name=Faux2007/><ref>{{usurped|1=[https://web.archive.org/web/20031230012958/http://www.davidkfaux.org/shetlandhaplogroupR1a.html Shetland Islands Haplogroups R1a & Q]}}</ref> On the other hand, it is 0.2% in [[Finland]],<ref>{{cite web|url=https://www.familytreedna.com/groups/finland/dna-results|title=Family Tree DNA – Genetic Testing for Ancestry, Family History & Genealogy}}</ref> 4.6% in [[Latvia]],<ref>{{cite web|url=https://www.familytreedna.com/public/Latvia/default.aspx?section=yresults|title=Family Tree DNA – My FamilyTree DNA Latvia Project Website}}</ref> 1.1% in [[Lithuania]],<ref>{{cite web|url=https://www.familytreedna.com/public/LithuanianDNA/default.aspx?section=yresults|title=Family Tree DNA – LITHUANIAN DNA}}</ref> 0.5% in [[Estonia]]. |
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====Western Europe==== |
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In [[Western Europe]], Q-M242 is observed at very low frequencies, around 0.5% in most of the countries, such as [[Germany]], [[France]], United Kingdom, etc., but some regions show a little higher. It is 2.1% in [[Switzerland]],<ref>{{cite web|url=https://www.familytreedna.com/public/switzerland/default.aspx?section=yresults|title=Family Tree DNA – Switzerland DNA Project}}</ref> and it reaches 5.1% in [[Lyon]] ([[Rhône-Alpes]]) region of France.<ref name=Wiik2008>{{cite journal|last1=Wiik|first1=Kalevi|year=2008|title=Where did European Men Come From?|journal=Journal of Genetic Genealogy|volume=4|pages=35–85}}</ref> It is about 4% in [[Shetland]] of northernmost Britain, with a place in it showing the highest figure at 8%. Shetland has been known to be a settlement of [[Vikings]]. And, surprisingly, Q-M242 in Shetland (also in some areas of [[Scandinavian Peninsula|Scandinavia]], Faroe Islands, Iceland, and the United Kingdom) has turned out to be generically closely linked to the Q-M242 in Central Asia. Also, Shetland (Norse) Q-M242 is revealed to be linked to some Q-M242 of [[Azerbaijanis|Azeris]] ([[Azerbaijan]]).<ref name=Faux2007>David K. Faux, 2007, The Genetic Link of the Viking – Era Norse to Central Asia: An Assessment of the Y Chromosome DNA, Archaeological, Historical and Linguistic Evidence, http://www.davidkfaux.org/CentralAsiaRootsofScandinavia-Y-DNAEvidence.pdf</ref> |
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====Southern Europe==== |
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[[Southern Europe]] also shows low frequencies of Q around 0.5%~1%, but some regions exhibits different figures. It is 1.9% in mainland [[Croatia]], but it reaches 14.3% (13/91) in [[Hvar]] Islands and 6.1% (8/132) in [[Korčula]].<ref name=Wiik2008/> Also, it is about 0.6% in [[Italy]], but it rises to 2.5% (6/236) in [[Sicily]], where it reaches 16.7% (3/18) in [[Mazara del Vallo]] region, followed by 7.1% (2/28) in [[Ragusa, Italy|Ragusa]], 3.6% in [[Sciacca]],<ref name=Gaetano2009>{{cite journal|last1=Di Gaetano|first1=Cornelia|display-authors=etal|date=Jan 2009|title=Differential Greek and northern African migrations to Sicily are supported by genetic evidence from the Y chromosome|journal=Eur J Hum Genet|volume=17|issue=1|pages=91–99|doi=10.1038/ejhg.2008.120|pmid=18685561|pmc=2985948}}</ref> and 3.7% in [[Belvedere Marittimo]].<ref>{{cite journal|last1=Brisighelli|first1=F|year=2012|title=Uniparental markers of contemporary Italian population reveals details on its pre-Roman heritage|journal=PLOS One|volume=7|issue=12|page=e50794|doi=10.1371/journal.pone.0050794|pmid=23251386|pmc=3519480|bibcode=2012PLoSO...750794B|doi-access=free}} In Table S4, #BEL50 is estimated to be Q-M378 by haplotype, though it is shown as just P* (xR1).</ref> |
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On the other hand, according to a study (Behar 2004), 5.2% (23/441) of [[Ashkenazi Jews|Ashkenazi Jewish]] males belong to haplogroup Q-P36.<ref name=Behar2004>{{cite journal|last1=Behar|first1=DM|display-authors=etal|date=Mar 2004|title=Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations|journal=Hum Genet|volume=114|issue=4|pages=354–65|doi=10.1007/s00439-003-1073-7|pmid=14740294|s2cid=10310338}}</ref> This has subsequently been found to be entirely the Q-M378 subclade and may be restricted to Q-L245. Also, 2.3% (4/174)<ref>{{cite journal|last1=Adams|first1=Susan M.|display-authors=etal|date=Dec 2008|title=The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula|journal=The American Journal of Human Genetics|volume=83|issue=6|pages=725–736|doi=10.1016/j.ajhg.2008.11.007|pmid=19061982|pmc=2668061}}</ref>~5.6% (3/53)<ref>Alain Farhi et al., Preliminary Results of Sephardic DNA Testing, AVOTAYNU Volume XXIII, Number 2 Summer 2007, p.10</ref> of [[Sephardi Jews]] are in haplogroup Q. |
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===Africa=== |
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Haplogroup Q is rarely found across [[North Africa]]. It is observed in 0.7% (1/147),<ref name=AbuAmero2009/> of [[Egyptians]] and in 0.6% (1/156)<ref name=Bekada2013/> of [[Demographics of Algeria|Algerian]] people. Surprisingly, it is also witnessed in 0.8% (3/381, all Q-M346) of males from [[Comoros]] which is located in between [[East Africa]] and [[Madagascar]]. |
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To combine the data above, Q-M242 is estimated to be in about 3.1% of males of the world. |
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===Subclade distribution=== |
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*'''Q (M242)''' |
*'''Q (M242)''' |
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**'''Q*''' |
**'''Q*''' – Found with low frequency in India and [[Pakistan]].<ref name="ycc"/> Important in [[Afghanistan]], paragroup Q-M242 (xMEH2, xM378) was found in eight [[Pashtuns|Pashtun]] males (3 [[Kabul]], 4 [[Laghman Province|Laghman]], 1 [[Kapisa (city)|Kapisa]]).<ref name="Haber2012">{{cite journal|vauthors=Haber M, Platt DE, Ashrafian Bonab M, Youhanna SC, Soria-Hernanz DF|display-authors=etal|year=2012|title=Afghanistan's Ethnic Groups Share a Y-Chromosomal Heritage Structured by Historical Events|journal=PLOS One|volume=7|issue=3|page=e34288|doi=10.1371/journal.pone.0034288|pmid=22470552|pmc=3314501|bibcode=2012PLoSO...734288H|doi-access=free}}</ref> Also found in one [[Rapanui]] male of [[Easter Island]].<ref>{{cite journal|pmid=17506287|doi=10.1353/hub.2007.0005|volume=78|issue=5|title=Y-chromosome-Specific STR haplotype data on the Rapanui population (Easter Island)|year=2006|journal=Hum Biol|pages=565–78|last1=Ghiani|first1=ME|last2=Moral|first2=P|last3=Mitchell|first3=RJ|last4=Hernández|first4=M|last5=García-Moro|first5=C|last6=Vona|first6=G|s2cid=33311525}}</ref> |
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**'''Q-P36.2''' (P36.2) Found with low frequency in [[Iran]].<ref>{{cite journal|last1=Grugni|first1=Viola|last2=Battaglia|first2=Vincenza|last3=Hooshiar Kashani|first3=Baharak|last4=Parolo|first4=Silvia|last5=Al-Zahery|first5=Nadia|last6=Achilli|first6=Alessandro|last7=Olivieri|first7=Anna|last8=Gandini|first8=Francesca|last9=Houshmand|first9=Massoud | last10 = Sanati | first10 = Mohammad Hossein|last11=Torroni|first11=Antonio|last12=Semino|first12=Ornella|year=2012|title=Ancient Migratory Events in the Middle East: New Clues from the Y-Chromosome Variation of Modern Iranians|journal=PLOS One|volume=7|issue=7|page=e41252|doi=10.1371/journal.pone.0041252|pmid=22815981|pmc=3399854|bibcode=2012PLoSO...741252G|doi-access=free}}</ref> |
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**'''Q1''' (P36.2) |
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***'''Q-MEH2''' (MEH2) Was found in [[Koryaks]] (at 10.3%), although the level of STR diversity associated with Q-MEH2 is very low, this lineage appears to be closest to the extinct [[Paleo-Eskimo]] individuals belonging to the [[Saqqaq culture]] arisen in the New World Arctic about 5.5 Ka.<ref>{{cite journal|doi=10.1038/jhg.2011.64|title=Ancient links between Siberians and Native Americans revealed by subtyping the Y chromosome haplogroup Q1a|year=2011|last1=Malyarchuk|first1=Boris|last2=Derenko|first2=Miroslava|last3=Denisova|first3=Galina|last4=Maksimov|first4=Arkady|last5=Wozniak|first5=Marcin|last6=Grzybowski|first6=Tomasz|last7=Dambueva|first7=Irina|last8=Zakharov|first8=Ilya|journal=Journal of Human Genetics|volume=56|issue=8|pages=583–8|pmid=21677663|doi-access=free}}</ref> |
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***'''Q1a''' (MEH2) |
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****'''[[Haplogroup Q-M120|Q-M120]]''' (M120, M265/N14) – It has been found at low frequency among [[Han Chinese]],<ref name="BoWen2004">{{cite journal|vauthors=Wen B, Li H, Lu D|display-authors=etal|title=Genetic evidence supports demic diffusion of Han culture|journal=Nature|volume=431|issue=7006|pages=302–5|date=September 2004|pmid=15372031|doi=10.1038/nature02878|bibcode=2004Natur.431..302W|s2cid=4301581}} – [http://www.nature.com/nature/journal/v431/n7006/extref/nature02878-s2.doc Supplementary Table 2: NRY haplogroup distribution in Han populations]</ref><ref name="BingSuHimalaya" /> [[Dungan people|Dungan]]s,<ref name="Wells2001" /> [[Nivkh people|Nivkhs]],<ref name="Kharkov2024">{{Cite journal|last=Kharkov|first=V. N.|last2=Kolesnikov|first2=N. A.|last3=Valikhova|first3=L. V.|last4=Zarubin|first4=A. A.|last5=Sukhomyasova|first5=A. L.|last6=Khitrinskaya|first6=I. Yu.|last7=Stepanov|first7=V. A.|date=2024-10-09|title=Traces of Paleolithic expansion in the Nivkh gene pool based on data on autosomal SNP and Y chromosome polymorphism|url=https://vavilov.elpub.ru/jour/article/view/4295|journal=Vavilov Journal of Genetics and Breeding|volume=28|issue=6|pages=659–666|doi=10.18699/vjgb-24-73|issn=2500-3259|pmc=11496309|pmid=39445096}}</ref> [[Koryaks]],<ref name="Kharkov2024" /> [[Yukaghir people|Yukaghirs]],<ref name="Kharkov2024" /> [[Vietnamese people|Vietnamese]],<ref name = "Poznik2016" /><ref name = "Macholdt2020" /> [[Japanese people|Japanese]],<ref name="Nonaka2007">{{cite journal|last1=Nonaka|first1=I.|last2=Minaguchi|first2=K.|last3=Takezaki|first3=N.|year=2007|title=Y-chromosomal Binary Haplogroups in the Japanese Population and their Relationship to 16 Y-STR Polymorphisms|url=http://ir.tdc.ac.jp/irucaa/bitstream/10130/491/1/j.1469-1809.2006.00343.x.pdf|journal=Annals of Human Genetics|volume=71|issue=4|pages=480–495|doi=10.1111/j.1469-1809.2006.00343.x|pmid=17274803|hdl=10130/491|s2cid=1041367|hdl-access=free}}</ref> [[Tuvans]],<ref name="Luis2023">>{{Cite journal|last=Luis|first=Javier Rodriguez|last2=Palencia-Madrid|first2=Leire|last3=Garcia-Bertrand|first3=Ralph|last4=Herrera|first4=Rene J.|date=2023-01-23|title=Bidirectional dispersals during the peopling of the North American Arctic|url=https://www.nature.com/articles/s41598-023-28384-8|journal=Scientific Reports|language=en|volume=13|issue=1|pages=1268|doi=10.1038/s41598-023-28384-8|issn=2045-2322|pmc=9871004|pmid=36690673}}</ref> [[Kalmyks]],<ref name = "Malyarchuk2013b">{{cite journal|last1=Malyarchuk|first1=Boris|last2=Derenko|first2=Miroslava|last3=Denisova|first3=Galina|last4=Khoyt|first4=Sanj|last5=Woźniak|first5=Marcin|last6=Grzybowski|first6=Tomasz|last7=Zakharov|first7=Ilya|year=2013|title=Y-chromosome diversity in the Kalmyks at the ethnical and tribal levels|journal=Journal of Human Genetics|volume=58|issue=12|pages=804–811|doi=10.1038/jhg.2013.108|pmid=24132124|doi-access=free}}</ref> [[Koreans]],<ref name="Wells2001">{{cite journal|last1=Wells|first1=R. Spencer|last2=Yuldasheva|first2=Nadira|last3=Ruzibakiev|first3=Ruslan|last4=Underhill|first4=Peter A.|last5=Evseeva|first5=Irina|last6=Blue-Smith|first6=Jason|last7=Jin|first7=Li|last8=Su|first8=Bing|last9=Pitchappan|first9=Ramasamy |last10=Shanmugalakshmi |first10=Sadagopal|last11=Balakrishnan|first11=Karuppiah|last12=Read|first12=Mark|last13=Pearson|first13=Nathaniel M.|last14=Zerjal|first14=Tatiana|last15=Webster|first15=Matthew T.|last16=Zholoshvili|first16=Irakli|last17=Jamarjashvili|first17=Elena|last18=Gambarov|first18=Spartak|last19=Nikbin|first19=Behrouz |last20=Dostiev |first20=Ashur|last21=Aknazarov|first21=Ogonazar|last22=Zalloua|first22=Pierre|last23=Tsoy|first23=Igor|last24=Kitaev|first24=Mikhail|last25=Mirrakhimov|first25=Mirsaid|last26=Chariev|first26=Ashir|last27=Bodmer|first27=Walter F.|title=The Eurasian Heartland: A continental perspective on Y-chromosome diversity|journal=Proceedings of the National Academy of Sciences of the United States of America|date=28 August 2001|volume=98|issue=18|pages=10244–10249|doi=10.1073/pnas.171305098|pmid=11526236|pmc=56946|bibcode=2001PNAS...9810244W|doi-access=free}}</ref> [[Mongols]] in [[Mongolia]],<ref name = "DiCristofaro2013">{{cite journal|last1=Di Cristofaro|first1=J|last2=Pennarun|first2=E|last3=Mazières|first3=S|last4=Myres|first4=NM|last5=Lin|first5=AA|display-authors=etal|year=2013|title=Afghan Hindu Kush: Where Eurasian Sub-Continent Gene Flows Converge|journal=PLOS One|volume=8|issue=10|page=e76748|doi=10.1371/journal.pone.0076748|pmid=24204668|pmc=3799995|bibcode=2013PLoSO...876748D|doi-access=free}}</ref> [[Tibetan people|Tibetans]],<ref name="BingSuHimalaya"/><ref name=Gayden2007/><ref name ="Wang2014">{{cite journal|last1=Wang C-C|first1=Wang L-X|last2=Shrestha|first2=R|last3=Zhang|first3=M|last4=Huang|first4=X-Y|display-authors=etal|year=2014|title=Genetic Structure of Qiangic Populations Residing in the Western Sichuan Corridor|journal=PLOS One|volume=9|issue=8|page=e103772|doi=10.1371/journal.pone.0103772|pmid=25090432|pmc=4121179|bibcode=2014PLoSO...9j3772W|doi-access=free}}</ref> and [[Hmong language|Hmong Daw]] in Laos.<ref name = "Cai2011">{{cite journal|last1=Cai|first1=X|last2=Qin|first2=Z|last3=Wen|first3=B|last4=Xu|first4=S|last5=Wang|first5=Y|last6=Lu|first6=Yan|last7=Wei|first7=Lanhai|last8=Wang|first8=Chuanchao|last9=Li|first9=Shilin | last10 = Huang | first10 = Xingqiu|last11=Jin|first11=Li|last12=Li|first12=Hui|year=2011|title=Human Migration through Bottlenecks from Southeast Asia into East Asia during Last Glacial Maximum Revealed by Y Chromosomes|journal=PLOS One|volume=6|issue=8|page=e24282|doi=10.1371/journal.pone.0024282|pmid=21904623|pmc=3164178|bibcode=2011PLoSO...624282C|doi-access=free}}</ref> It also has been reported in samples of [[demographics of Bhutan|Bhutanese]],<ref name = "Hallast2014">{{cite journal|last1=Hallast|first1=Pille|last2=Batini|first2=Chiara|last3=Zadik|first3=Daniel|display-authors=etal|year=2014|title=The Y-Chromosome Tree Bursts into Leaf: 13,000 High-Confidence SNPs Covering the Majority of Known Clades|journal=Molecular Biology and Evolution|volume=32|issue=3|pages=661–673|doi=10.1093/molbev/msu327|pmid=25468874|doi-access=free|pmc=4327154}}</ref> [[Hazaras|Hazara]],<ref name="Sengupta2006">{{cite journal|last1=Sengupta|first1=Sanghamitra|last2=Zhivotovsky|first2=Lev A.|last3=King|first3=Roy|last4=Mehdi|first4=S.Q.|last5=Edmonds|first5=Christopher A.|last6=Cheryl-|first6=Cheryl-Emiliane T.|last7=Chow|first7=Emiliane T.|last8=Lin|first8=Alice A.|last9=Mitra|first9=Mitashree | last10 = Ramesh | first10 = A.|last11=Usha Rani|first11=M.V.|last12=Thakur|first12=Chitra M.|last13=Cavalli-Sforza|first13=L. Luca|last14=Majumder|first14=Partha P.|last15=Underhill|first15=Peter A.|year=2006|title=Polarity and Temporality of High-Resolution Y-Chromosome Distributions in India Identify Both Indigenous and Exogenous Expansions and Reveal Minor Genetic Influence of Central Asian Pastoralists|journal=The American Journal of Human Genetics|volume=78|issue=2|pages=202–221|doi=10.1086/499411|display-authors=8|pmid=16400607|pmc=1380230}}</ref> Bruneian [[Murut people|Murut]],<ref name = "Karmin2015">Monika Karmin, Lauri Saag, Mário Vicente, ''et al''. (2015), "A recent bottleneck of Y chromosome diversity coincides with a global change in culture." ''Genome Research'' 25:1–8. Published by Cold Spring Harbor Laboratory Press; ISSN 1088-9051/15; www.genome.org.</ref> [[Gurjar|Gujar]],<ref name=Sharma2007/> [[Baloch people|Baloch]],<ref name=Grugni2012 /> [[Georgians|Georgian]],<ref name="Alborova2016">{{Cite journal|last1=Alborova|first1=I.E.|last2=Pocheshkhova|first2=E.A.|last3=Chikovani|first3=N.L.|last4=Dibirova|first4=K.D.|display-authors=1|date=October 2016|title=FEATURES OF THE GENE POOL LAZ AND IMERETIANSS ACCORDING ABOUT Y-CHROMOSOME POLYMORPHISMS|url=https://science-education.ru/en/article/view?id=25241|journal=Modern Problems of Science and Education|pages=315}}</ref> and [[Peru]]vian<ref name = "Poznik2016" /> populations. |
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****'''Q1a*''' Was found in [[Koryaks]] (at 10.3%), although the level of STR diversity associated with Q1a*-MEH2 is very low, this lineage appears to be closest to the extinct [[Palaeo-Eskimo]] individuals belonging to the [[Saqqaq culture]] arisen in the New World Arctic about 5.5 Ka.<ref>{{cite journal |doi=10.1038/jhg.2011.64 |title=Ancient links between Siberians and Native Americans revealed by subtyping the Y chromosome haplogroup Q1a |year=2011 |last1=Malyarchuk |first1=Boris |last2=Derenko |first2=Miroslava |last3=Denisova |first3=Galina |last4=Maksimov |first4=Arkady |last5=Wozniak |first5=Marcin |last6=Grzybowski |first6=Tomasz |last7=Dambueva |first7=Irina |last8=Zakharov |first8=Ilya |journal=Journal of Human Genetics |volume=56 |issue=8 |pages=583–8 |pmid=21677663}}</ref> |
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****'''[[Haplogroup Q-M25|Q-M25]]''' (M25, M143) – Found with high frequency of 30-45% in Turkmens and Turkmenistan Confused with R1b1 because of P25. Found with high frequency in [[Turkmens]] of [[Golestan province]] ([[Iran]]),<ref name = "Grugni2012" /> [[Jowzjan Province|Jawzjan]] ( [[Afghanistan]]),<ref name = "DiCristofaro2013" /> and with low to moderate frequency in [[Lebanon]],<ref name="ZallouaLebanon">{{cite journal|doi=10.1016/j.ajhg.2008.01.020|last1=Zalloua|first1=Pierre A.|last2=Xue|first2=Y|year=2008|last3=Khalife|first3=J|last4=Makhoul|first4=N|last5=Debiane|first5=L|last6=Platt|first6=DE|last7=Royyuru|first7=AK|last8=Herrera|first8=RJ|last9=Hernanz|first9=DF |last10=Blue-Smith |first10=Jason|last11=Wells|first11=R. Spencer|last12=Comas|first12=David|last13=Bertranpetit|first13=Jaume|last14=Tyler-Smith|first14=Chris|last15=Genographic Consortim|title=Y-Chromosomal Diversity in Lebanon Is Structured by Recent Historical Events|journal=American Journal of Human Genetics|volume=82|issue=4|pages=873–882|pmid=18374297|pmc=2427286|display-authors=8}}</ref> [[Mongolia]],<ref name = "DiCristofaro2013" /> and [[Turkey]]<ref name="Cinnioglu2004" /> |
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****'''Q1a1''' (M120, M265/N14) — ''It is so far restricted to East Asia. It has been found at low frequency among [[Han Chinese]],<ref name="BoWen2004">{{cite journal |author=Wen B, Li H, Lu D, ''et al'' |title=Genetic evidence supports demic diffusion of Han culture |journal=Nature |volume=431 |issue=7006 |pages=302–5 |year=2004 |month=September |pmid=15372031 |doi=10.1038/nature02878 |url=http://www.nature.com/nature/journal/v431/n7006/abs/nature02878.html |quote=[http://www.nature.com/nature/journal/v431/n7006/extref/nature02878-s2.doc Supplementary Table 2: NRY haplogroup distribution in Han populations]}}</ref><ref name = "BingSuHimalaya" /> [[Dungan people|Dungan]]s,<ref name = "Wells2001" /> [[Japanese people|Japanese]],<ref name = "Nonaka2007">I. Nonaka, K. Minaguchi, and N. Takezaki, "Y-chromosomal Binary Haplogroups in the Japanese Population and their Relationship to 16 Y-STR Polymorphisms," ''Annals of Human Genetics'' Volume 71 Issue 4, Pages 480 - 495 (July 2007).</ref> [[Koreans]],<ref name = "Wells2001">{{cite journal |author=Wells RS, Yuldasheva N, Ruzibakiev R, ''et al'' |title=The Eurasian Heartland: A continental perspective on Y-chromosome diversity |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=98 |issue=18 |pages=10244–9 |year=2001 |month=August |pmid=11526236 |pmc=56946 |doi=10.1073/pnas.171305098 |quote=[http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=56946&rendertype=table&id=T1 Table 1: Y-chromosome haplotype frequencies in 49 Eurasian populations, listed according to geographic region]}}</ref> and [[Tibetans]].<ref name="Gayden2007">{{cite journal |author=Gayden T, Cadenas AM, Regueiro M, ''et al'' |title=The Himalayas as a Directional Barrier to Gene Flow |journal=Am. J. Hum. Genet. |volume=80 |issue=5 |pages=884–94 |year=2007 |month=May |pmid=17436243 |pmc=1852741 |doi=10.1086/516757 }}</ref><ref name = "BingSuHimalaya" /> Although it was reported in the [[Hazara people|Hazaras]],<ref name = "Sengupta2006">Sanghamitra Sengupta, Lev A. Zhivotovsky, Roy King, S.Q. Mehdi, Christopher A. Edmonds, Cheryl-Emiliane T. Chow, Alice A. Lin, Mitashree Mitra, Samir K. Sil, A. Ramesh, M.V. Usha Rani, Chitra M. Thakur, L. Luca Cavalli-Sforza, Partha P. Majumder, and Peter A. Underhill, "Polarity and Temporality of High-Resolution Y-Chromosome Distributions in India Identify Both Indigenous and Exogenous Expansions and Reveal Minor Genetic Influence of Central Asian Pastoralists," ''The American Journal of Human Genetics'', Volume 78, Issue 2, 202-221, 1 February 2006.</ref> it was subsequently shown to be a lab error as demonstrated by the phylogenetic tree changes in Karafet 2008. |
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****'''[[Haplogroup Q-M346|Q-M346]]''' (L56, L57, M346) – Found at low frequency in Europe, South Asia and West Asia. It has been found in [[Pakistan]],<ref name="Sengupta2006" /> [[Iran]],<ref name = "DiCristofaro2013" /> [[Afghanistan]],<ref name = "DiCristofaro2013" /> [[Kyrgyzstan]],<ref name = "DiCristofaro2013" /> [[Saudi Arabia]],<ref name="AbuAmero2009" /> the [[United Arab Emirates]],<ref name="Cadenas2008"/> India,<ref name="Sengupta2006" /> [[Mongolia]],<ref name = "DiCristofaro2013" /> [[Tibetans|Tibet]],<ref name=Gayden2007/> and [[Balinese people|Bali]].<ref name = "Karafet2010">{{cite journal|last1=Karafet|first1=Tatiana M.|last2=Hallmark|first2=Brian|last3=Cox|first3=Murray P.|display-authors=etal|year=2010|title=Major East–West Division Underlies Y Chromosome Stratification across Indonesia|journal=Mol. Biol. Evol.|volume=27|issue=8|pages=1833–1844|doi=10.1093/molbev/msq063|pmid=20207712|doi-access=free}}</ref> |
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****'''Q1a2''' (M25, M143) — ''Found with low to moderate frequency in [[Iran]],<ref name =Regueiro2006 /> [[Lebanon]],<ref name = "ZallouaLebanon">{{cite journal | doi = 10.1016/j.ajhg.2008.01.020 | last1 = Zalloua | first1 = Pierre A. | author-separator =, | last2 = Xue | author-name-separator= | first2 = Y| year = 2008 | last3 = Khalife | first3 = J | last4 = Makhoul | first4 = N | last5 = Debiane | first5 = L | last6 = Platt | first6 = DE | last7 = Royyuru | first7 = AK | last8 = Herrera | first8 = RJ | last9 = Hernanz | first9 = DF| title = Y-Chromosomal Diversity in Lebanon Is Structured by Recent Historical Events | url = | journal = American Journal of Human Genetics | volume = 82 | issue = 4| pages = 873–882 | pmid = 18374297 | pmc = 2427286 }}</ref> and [[Turkey]]<ref name="Cinnioglu2004" />'' |
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*****'''Q-L53''' (L53, L54, L55, L213) |
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****[[Haplogroup Q1a3 (Y-DNA)|'''Q1a3''']] (L56, L57, M346) — ''Found at low frequency in Europe, South Asia and West Asia. Including its Q-M3 subclade, it is the only branch of haplogroup Q found in modern indigenous populations of the Americas. It has been found in [[Pakistan]],<ref name = "Sengupta2006" /> [[Saudi Arabia]],<ref name = "AbuAmero2009" /> the [[United Arab Emirates]],<ref name="Cadenas2008"/> [[India]] <ref name = "Sengupta2006" /> and [[Tibetans|Tibet]].<ref name=Gayden2007/> |
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******'''[[Haplogroup Q-M3|Q-M3]]''' ('''M3''') – Common in [[indigenous peoples of the Americas]]<ref name=Genebase>{{cite web|title=Learn about Y-DNA Haplogroup Q|work=Wendy Tymchuk – Senior Technical Editor|url=http://www.genebase.com/tutorial/item.php?tuId=16|publisher=Genebase Systems|year=2008|access-date=2009-11-21|url-status=dead|archive-url=https://web.archive.org/web/20100622001311/http://www.genebase.com/tutorial/item.php?tuId=16|archive-date=2010-06-22}}</ref> |
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*****'''Q1a3a''' (L53, L54, L55, L213) |
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*******Q-M19 (M19) – Found among some indigenous peoples of [[South America]], such as the [[Ticuna people|Ticuna]] and the [[Wayuu people|Wayuu]]<ref name="Bortolini2003"/> |
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******[[Haplogroup Q1a3a1 (Y-DNA)|'''Q1a3a1''']] ('''M3''') — ''Common in [[indigenous peoples of the Americas]]''<ref name=Genebase>{{cite web|title=Learn about Y-DNA Haplogroup Q |work=Wendy Tymchuk - Senior Technical Editor |url=http://www.genebase.com/tutorial/item.php?tuId=16|format=Verbal tutorial possible |publisher=Genebase Systems |year=2008|accessdate=2009-11-21}}</ref> |
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*******Q-M194 (M194) – In South America |
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*******Q1a3a1a (M19) — ''Found among some indigenous peoples of [[South America]], such as the [[Ticuna people|Ticuna]] and the [[Wayuu people|Wayuu]]''<ref>{{cite journal |author=Bortolini MC, Salzano FM, Thomas MG, ''et al'' |title=Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas |journal=Am. J. Hum. Genet. |volume=73 |issue=3 |pages=524–39 |year=2003 |month=September |pmid=12900798 |pmc=1180678 |doi=10.1086/377588 |url=http://www.ucl.ac.uk/tcga/tcgapdf/Bortolini-AJHG-03-YAmer.pdf}}</ref> |
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******* |
*******Q-M199 (M199, P106, P292) – In South America |
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*****'''[[Haplogroup Q-M323|Q-M323]]''' (M323) – It has been detected in [[Yemenite Jews]].<ref name="Shen2004">{{cite journal|doi=10.1002/humu.20077|title=Reconstruction of patrilineages and matrilineages of Samaritans and other Israeli populations from Y-Chromosome and mitochondrial DNA sequence Variation|year=2004|last1=Shen|first1=Peidong|last2=Lavi|first2=Tal|last3=Kivisild|first3=Toomas|last4=Chou|first4=Vivian|last5=Sengun|first5=Deniz|last6=Gefel|first6=Dov|last7=Shpirer|first7=Issac|last8=Woolf|first8=Eilon|last9=Hillel|first9=Jossi|last10=Feldman|first10=Marcus W.|last11=Oefner|first11=Peter J.|journal=Human Mutation|volume=24|issue=3|pages=248–60|pmid=15300852|s2cid=1571356|display-authors=8}} Q-M323 in 3/20=15% of a sample of Yemenite Jews.</ref> |
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*******Q1a3a1c (M199, P106, P292) — In South America |
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***'''[[Haplogroup Q-L275|Q-L275]]''' (L275, L314) |
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*****'''Q1a3b''' (M323) — ''It has been detected in [[Yemenite Jews]].<ref name = "Shen2004">{{cite journal |doi=10.1002/humu.20077 |title=Reconstruction of patrilineages and matrilineages of Samaritans and other Israeli populations from Y-Chromosome and mitochondrial DNA sequence Variation |year=2004 |last1=Shen |first1=Peidong |last2=Lavi |first2=Tal |last3=Kivisild |first3=Toomas |last4=Chou |first4=Vivian |last5=Sengun |first5=Deniz |last6=Gefel |first6=Dov |last7=Shpirer |first7=Issac |last8=Woolf |first8=Eilon |last9=Hillel |first9=Jossi |journal=Human Mutation |volume=24 |issue=3 |pages=248–60 |pmid=15300852}} ''Q-M323 in 3/20 = 15% of a sample of Yemenite Jews.''</ref> |
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****'''Q-M378''' (M378) – It is widely distributed in Europe, South Asia, West and East Asia. It is found among samples of [[Hazaras]] and [[Sindhis]].<ref name=Sengupta2006 /> It is also found in the [[Mongols]], the [[Japanese people]] and the [[Uyghurs]] of North-Western China in two separate groups.<ref name=Zhong2010>{{cite journal|doi=10.1093/molbev/msq247|title=Extended Y Chromosome Investigation Suggests Postglacial Migrations of Modern Humans into East Asia via the Northern Route|year=2010|last1=Zhong|first1=H.|last2=Shi|first2=H.|last3=Qi|first3=X.-B.|last4=Duan|first4=Z.-Y.|last5=Tan|first5=P.-P.|last6=Jin|first6=L.|last7=Su|first7=B.|last8=Ma|first8=R. Z.|journal=Molecular Biology and Evolution|volume=28|pages=717–27|pmid=20837606|issue=1|doi-access=free}}</ref> The Q-M378 subclade is a branch to which Q-M242 men in some European Jewish Diaspora populations belong. Its subbranch Q-L245's subclades Q-Y2200 and Q-YP1035 are found in [[Ashkenazi Jews]].<ref>Brook, Kevin Alan (2018). ''The Jews of Khazaria'' (3rd ed.), p. 204. [[Rowman & Littlefield]].</ref> Some [[Sephardic Jews]] carry other subclades of Q-L245, including Q-BZ3900, Q-YP745, and Q-YP1237. Q-M378 samples also have been located in [[Central America]] ([[Panama]]) and [[South America]] ([[Andes|Andean Region]])<ref name="Battaglia2013"/> |
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***'''Q1b''' (L275, L314) |
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****'''Q1b1''' (M378) — ''It is widely distributed in Europe, South Asia, and West Asia. It is found among samples of [[Hazara people|Hazaras]] and [[Sindhi people|Sindhis]].<ref name=Sengupta2006 /> It is also found in the [[Uyghur people|Uyghurs]] of North-Western [[China]] in two separate groups.<ref name=Zhong2010>{{cite journal |doi=10.1093/molbev/msq247 |title=Extended Y Chromosome Investigation Suggests Postglacial Migrations of Modern Humans into East Asia via the Northern Route |year=2010 |last1=Zhong |first1=H. |last2=Shi |first2=H. |last3=Qi |first3=X.-B. |last4=Duan |first4=Z.-Y. |last5=Tan |first5=P.-P. |last6=Jin |first6=L. |last7=Su |first7=B. |last8=Ma |first8=R. Z. |journal=Molecular Biology and Evolution |volume=28 |pages=717–27 |pmid=20837606 |issue=1}}</ref> The Q-M378 subclade and specifically its Q-L245 subbranch is speculated to be the branch to which Q-M242 men in Jewish Diaspora populations belong.<ref name=behar /><ref name=adams >{{cite journal | doi = 10.1016/j.ajhg.2008.11.007 | last1 = Adams | first1 = S. M. | last2 = Bosch | first2 = E. | last3 = Balaresque | first3 = P. L. | last4 = Ballereau | first4 = S. J. | last5 = Lee | first5 = A. C. | last6 = Arroyo | first6 = E. | last7 = López-Parra | first7 = A. M. | last8 = Aler | first8 = M. | last9 = Grifo | first9 = M. S. ''et al.'' | year = 2008 | title = The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula | url = | journal = Am J Hum Genet | volume = 83 | issue = 6| pages = 725–736 | pmid = 19061982 | pmc = 2668061 }}</ref> Although published articles have not tested for M378 in Jewish populations, [[Genetic genealogy|genetic genealogists]] from the [[Ashkenazi]], [[Mizrahi Jews|Mizrachi]], and [[Sephardi]] Jewish populations have tested positive for both M378 and L245. |
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==Y-DNA Q samples from ancient sites== |
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{{Main|List of haplogroups of historic people}} |
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* South Central Siberia (near Altai) |
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** Afontova-Gora-2, [[Yenisei River]] Bank, [[Krasnoyarsk]] (South Central Siberia of Russia), 17000YBP: Q1a1-F1215 (mtDNA R)<ref>[http://snag.gy/S1RSQ.jpg YFull – Experimental Y Tree], [https://genetiker.wordpress.com/2014/05/28/y-snp-calls-for-afontova-gora-2/ Y-SNP calls for Afontova Gora 2], [http://www.anthrogenica.com/showthread.php?2645-Afantova-had-haplogroup-Q1a1-and-some-type-of-R-derived-mtdna Afantova had haplogroup Q1a1 and some type of R derived mtdna.]</ref> |
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* North America |
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** [[Anzick-1]], [[Clovis culture]], western [[Montana]], 12600YBP: Q1a2-L54* (not M3, mtDNA D4h3a)<ref>{{cite journal|last1=Rasmussen|first1=M.|last2=Anzick|first2=S.|display-authors=etal|title=The genome of a Late Pleistocene human from a Clovis burial site in western Montana|journal=Nature|volume=506|issue=7487|pages=225–229|doi=10.1038/nature13025|pmid=24522598|date=February 2014|pmc=4878442|bibcode=2014Natur.506..225R}}</ref><ref>{{cite journal|last1=Raff|first1=Jennifer A.|last2=Bolnick|first2=Deborah A.|title=Genetic roots of the first Americans|journal=Nature|date=February 2014|volume=506|issue=7487|pages=162–163|doi=10.1038/506162a|pmid=24522593|s2cid=4445278|doi-access=free}}</ref> |
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** [[Kennewick Man]], [[Washington (state)|Washington]], 8500YBP: Q1a2-M3 (mtDNA X2a)<ref>{{Cite journal|doi=10.1038/nature14625|pmid=26087396|pmc=4878456|title=The ancestry and affiliations of Kennewick Man|journal=Nature|volume=523|issue=7561|pages=455–458|year=2015|last1=Rasmussen|first1=Morten|last2=Sikora|first2=Martin|last3=Albrechtsen|first3=Anders|last4=Korneliussen|first4=Thorfinn Sand|last5=Moreno-Mayar|first5=J. Víctor|last6=Poznik|first6=G. David|last7=Zollikofer|first7=Christoph P. E.|last8=Ponce De León|first8=Marcia S.|last9=Allentoft|first9=Morten E.| last10=Moltke| first10=Ida|last11=Jónsson|first11=Hákon|last12=Valdiosera|first12=Cristina|last13=Malhi|first13=Ripan S.|last14=Orlando|first14=Ludovic|last15=Bustamante|first15=Carlos D.|last16=Stafford|first16=Thomas W.|last17=Meltzer|first17=David J.|last18=Nielsen|first18=Rasmus|last19=Willerslev|first19=Eske|bibcode=2015Natur.523..455R}}</ref> |
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* [[Altai Mountains|Altai]] (West Mongolia) |
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** Tsagaan Asga and Takhilgat Uzuur-5 [[Kurgan]] sites, westernmost Mongolian Altai, 2900YBP-4800YBP: 4 R1a1a1b2-Z93 (B.C. 10C, B.C. 14C, 2 period unknown), 3 Q1a2a1-L54 (period unknown), 1 Q-M242 (B.C. 28C), 1 C-M130 (B.C. 10C)<ref>Hollard et al., Strong genetic admixture in the Altai at the Middle Bronze Age revealed by uniparental and ancestry informative makers, Forensic Science International: Genetics, published online 4 June 2014</ref> |
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* Greenland |
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** [[Saqqaq]] ([[Qilakitsoq]]), [[Greenland]], 4000YBP: Q1a-YP1500<ref>{{cite web|url=https://yfull.com/tree/Q-YP1500/|title=Q-YP1500 YTree}}</ref> (mtDNA D2a1)<ref name=pmid20148029/> |
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* China |
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** Hengbei site (Peng kingdom cemetery of [[Western Zhou]] period), [[Jiang County]], [[Shanxi]], 2800-3000YBP: 9 Q1a1-M120, 2 O2a-M95, 1 N, 4 O3a2-P201, 2 O3, 4 O*<ref name="Henbei, Pengyang 2012">On Henbei, Pengyang, and Heigouliang, Lihongjie, Y-Chromosome Genetic Diversity of the Ancient North Chinese populations, Jilin University-China (2012)</ref> |
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***In another paper, the social status of those human remains of ancient Peng kingdom(倗国) are analyzed. aristocrats: 3 Q1a1 (prostrate 2, supine 1), 2 O3a (supine 2), 1 N (prostrate) / commoners : 8 Q1a1 (prostrate 4, supine 4), 3 O3a (prostrate 1, supine 2), 3 O* (supine 3) / slaves: 3 O3a, 2 O2a, 1 O*<ref>{{cite journal|last1=Zhao|first1=Yong-Bin|last2=Zhang|first2=Ye|last3=Li|first3=Hong-Jie|last4=Cui|first4=Ying-Qiu|last5=Zhu|first5=Hong|last6=Zhou|first6=Hui|title=Ancient DNA evidence reveals that the Y chromosome haplogroup Q1a1 admixed into the Han Chinese 3,000 years ago|journal=American Journal of Human Biology|date=November 2014|volume=26|issue=6|pages=813–821|doi=10.1002/ajhb.22604|pmid=25130911|s2cid=20553478}}</ref> |
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*** (cf) Pengbo (倗伯), Monarch of Peng Kingdom is estimated as Q-M120. |
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** [[Pengyang County]], [[Ningxia]], 2500YBP: all 4 Q1a1-M120<ref name="Henbei, Pengyang 2012"/> (with a lot of animal bones and bronze swords and other weapons, etc.) |
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** Heigouliang, [[Xinjiang]], 2200YBP: 6 Q1a* (not Q1a1-M120, not Q1a1b-M25, not Q1a2-M3), 4 Q1b-M378, 2 Q* (not Q1a, not Q1b: unable to determine subclades):<ref>Lihongjie, Y-Chromosome Genetic Diversity of the Ancient North Chinese populations, Jilin University-China (2012)</ref> |
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*** In a paper (Lihongjie 2012), the author analyzed the Y-DNAs of the ancient male samples from the 2nd or 1st century BCE cemetery at [[Heigouliang]] in Xinjiang – which is also believed to be the site of a summer palace for [[Xiongnu]] kings – which is east of the Barkol basin and near the city of [[Hami City|Hami]]. The Y-DNA of 12 men excavated from the site belonged to Q-MEH2 (Q1a) or Q-M378 (Q1b). The Q-M378 men among them were regarded as hosts of the tombs; half of the Q-MEH2 men appeared to be hosts and the other half as sacrificial victims. |
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**[[Xiongnu]] site in Barkol, Xinjiang, all 3 Q-M3 |
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***In L. L. Kang et al. (2013), three samples from a Xiongnu) site in [[Barköl Kazakh Autonomous County|Barkol]], Xinjiang were found to be Q-M3 (Q1a2a1a1). And, as Q-M3 is mostly found in Yeniseians and Native Americans, the authors suggest that the Xiongnu had connections to speakers of the [[Yeniseian languages]].<ref>L. L. Kang et al., Y chromosomes of ancient Hunnu people and its implication on the phylogeny of East Asian linguistic families (2013)</ref><ref>Knowing the Xiongnu Culture in Eastern Tianshan Mountain from Tomb Heigouliang and Dongheigou Site at the Beginning of Xihan Dynasty, RenMeng, WangJianXin, 2008</ref> These discoveries from the above papers (Li 2012, Kang et al., 2013) have some positive implications on the not as yet clearly verified theory that the Xiongnu were precursors of the [[Huns]]. |
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** Mongolian noble burials in the [[Yuan dynasty]], Shuzhuanglou Site, northernmost [[Hebei]] China, 700YBP: all 3 Q (not analysed subclade, the principal occupant Gaodangwang Korguz (高唐王=趙王 阔里吉思)'s mtDNA=D4m2, two others mtDNA=A)<ref>{{cite journal|last1=Qui|first1=Y|display-authors=etal|year=2015|title=Identification of kinship and occupant status in Mongolian noble burials of the Yuan dynasty through a multidisciplinary approach|journal=Phil. Trans. R. Soc.|volume=B370|issue=1660|page=20130378|doi=10.1098/rstb.2013.0378|pmid=25487330|pmc=4275886}}</ref> |
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***(cf) [[George (Ongud king)|Korguz]] was a son of a princess of [[Kublai Khan]] (元 世祖), and was the king of the [[Ongud]] tribe. He died in 1298 and was reburied in Shuzhuanglou in 1311 by his son. (Do not confuse this man with the Uyghur governor, [[Korguz]] who died in 1242.) The Ongud tribe (汪古部) was a descendant of the [[Shatuo]] tribe (沙陀族) which was a tribe of [[Göktürks]] ([[Western Turkic Khaganate]]) and was prominent in the [[Five Dynasties and Ten Kingdoms period]] of China, building three dynasties. His two queens were all princesses of the Yuan dynasty (Kublai Khan's granddaughters). It was very important for the Yuan dynasty to maintain a marriage alliance with Ongud tribe which had been a principal assistant since [[Genghis Khan]]'s period. About 16 princesses of the Yuan dynasty married kings of the Ongud tribe. |
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==See also== |
==See also== |
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===Populations=== |
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{{columns-list|colwidth=22em| |
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**[[Indigenous peoples of the Americas]] |
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*[[Paleo-Indians]] |
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*[[Indigenous peoples of the Americas]] |
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**[[Hazara people|Hazara]] |
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*[[Ket people]] |
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*[[Selkup people]] |
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*[[Siberian Tatars]] |
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*[[Inuit]] |
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*[[Chukchi people]] |
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**[[Ethnic groups of South Asia|Indian populations]] |
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*[[Akha people]] |
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*[[Turkmens]] |
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*[[Y-DNA haplogroups in populations of South Asia]] |
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*[[Genetics and archaeogenetics of South Asia]] |
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*[[Paragroup]] |
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}} |
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===Y-DNA Q-M242 subclades=== |
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*'''Genetics''' |
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{{columns-list|colwidth=22em| |
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**[[Haplogroup]] |
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*Q-M242 |
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**[[Haplotype]] |
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*[[Haplogroup Q-NWT01|Q-NWT01]] |
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**[[Subclade]] |
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*[[Haplogroup Q-M120|Q-M120]] |
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**[[Paragroup]] |
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*[[Haplogroup Q-B143|Q-B143]] |
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*[[Haplogroup Q-M25|Q-M25]] |
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*'''Subclades''' |
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*[[Haplogroup Q-M346|Q-M346]] |
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*[[Haplogroup Q-L53|Q-L53]] |
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*[[Haplogroup Q-L54|Q-L54]] |
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*[[Haplogroup Q-M3|Q-M3]] |
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*[[Haplogroup Q-M323|Q-M323]] |
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*[[Haplogroup Q-P89.1|Q-P89.1]] |
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*[[Haplogroup Q-Z780|Q-Z780]] |
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*[[Haplogroup Q-L275|Q-L275]] |
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}} |
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===Y-DNA backbone tree=== |
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{{Y-DNA}} |
{{Y-DNA}} |
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==References== |
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== External links == |
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{{Reflist}} |
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*[http://www.qydna.org Q Y-Haplogroup Project] at [[FTDNA]] |
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*[http://www.familytreedna.com/public/Amerind%20Y/index.aspx?fixed_columns=on American Indian Q3 project] at [[FTDNA]] |
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===Bibliography=== |
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*[https://www3.nationalgeographic.com/genographic/atlas.html?card=my045 Spread of Haplogroup Q], from [[The Genographic Project]], ''[[National Geographic (magazine)|National Geographic]]'' |
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{{Div col|colwidth=30em}} |
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*{{Cite journal|doi=10.1186/1471-2156-10-59|title=Saudi Arabian Y-Chromosome diversity and its relationship with nearby regions|year=2009|last1=Abu-Amero|first1=Khaled K|last2=Hellani|first2=Ali|last3=González|first3=Ana M|last4=Larruga|first4=Jose M|last5=Cabrera|first5=Vicente M|last6=Underhill|first6=Peter A|journal=BMC Genetics|volume=10|pages=59|pmid=19772609|pmc=2759955|issue=1|doi-access=free}} |
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*{{Cite journal|doi=10.1007/s00439-003-1073-7|title=Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations|year=2004|last1=Behar|first1=Doron M.|last2=Garrigan|first2=Daniel|last3=Kaplan|first3=Matthew E.|last4=Mobasher|first4=Zahra|last5=Rosengarten|first5=Dror|last6=Karafet|first6=Tatiana M.|last7=Quintana-Murci|first7=Lluis|last8=Ostrer|first8=Harry|last9=Skorecki|first9=Karl|last10=Hammer|first10=Michael F.|journal=Human Genetics|volume=114|pages=354–65|pmid=14740294|issue=4|s2cid=10310338|display-authors=8}} |
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*{{Cite journal|doi=10.1086/377588|title=Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas|year=2003|last1=Bortolini|first1=M|last2=Salzano|first2=F|last3=Thomas|first3=M|last4=Stuart|first4=S|last5=Nasanen|first5=S|last6=Bau|first6=C|last7=Hutz|first7=M|last8=Layrisse|first8=Z|last9=Petzlerler|first9=M|last10=Tsuneto|first10=L|last11=Hill|first11=K|last12=Hurtado|first12=A. M.|last13=Castro-De-Guerra|first13=D|last14=Torres|first14=M. M.|last15=Groot|first15=H|last16=Michalski|first16=R|last17=Nymadawa|first17=P|last18=Bedoya|first18=G|last19=Bradman|first19=N|last20=Labuda|first20=D|last21=Ruiz-Linares|first21=A|journal=The American Journal of Human Genetics|volume=73|pages=524–39|pmid=12900798|issue=3|pmc=1180678|display-authors=8}} |
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*{{Cite journal|doi=10.1038/sj.ejhg.5201934|title=Y-chromosome diversity characterizes the Gulf of Oman|year=2007|last1=Cadenas|first1=Alicia M|last2=Zhivotovsky|first2=Lev A|last3=Cavalli-Sforza|first3=Luca L|last4=Underhill|first4=Peter A|last5=Herrera|first5=Rene J|journal=European Journal of Human Genetics|volume=16|pages=374–86|pmid=17928816|issue=3|doi-access=free}}*{{Cite journal|doi=10.1038/sj.ejhg.5201934|title=Y-chromosome diversity characterizes the Gulf of Oman|year=2007|last1=Cadenas|first1=Alicia M|last2=Zhivotovsky|first2=Lev A|last3=Cavalli-Sforza|first3=Luca L|last4=Underhill|first4=Peter A|last5=Herrera|first5=Rene J|journal=European Journal of Human Genetics|volume=16|pages=374–86|pmid=17928816|issue=3|doi-access=free}} |
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*{{Cite journal|doi=10.1007/s00439-003-1031-4|title=Excavating Y-chromosome haplotype strata in Anatolia|year=2004|last1=Cinnioglu|first1=Cengiz|last2=King|first2=Roy|last3=Kivisild|first3=Toomas|last4=Kalfoglu|first4=Ersi|last5=Atasoy|first5=Sevil|last6=Cavalleri|first6=Gianpiero L.|last7=Lillie|first7=Anita S.|last8=Roseman|first8=Charles C.|last9=Lin|first9=Alice A.|last10=Prince|first10=Kristina|last11=Oefner|first11=Peter J.|last12=Shen|first12=Peidong|last13=Semino|first13=Ornella|last14=Cavalli-Sforza|first14=L. Luca|last15=Underhill|first15=Peter A.|journal=Human Genetics|volume=114|pages=127–48|pmid=14586639|issue=2|s2cid=10763736|display-authors=8}} |
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*{{Cite journal|doi=10.1038/sj.ejhg.5201726|title=Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan|year=2006|last1=Firasat|first1=Sadaf|last2=Khaliq|first2=Shagufta|last3=Mohyuddin|first3=Aisha|last4=Papaioannou|first4=Myrto|last5=Tyler-Smith|first5=Chris|last6=Underhill|first6=Peter A|last7=Ayub|first7=Qasim|journal=European Journal of Human Genetics|volume=15|pages=121–6|pmid=17047675|issue=1|pmc=2588664}} |
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*{{Cite journal|doi=10.1086/516757|title=The Himalayas as a Directional Barrier to Gene Flow|year=2007|last1=Gayden|first1=T|journal=The American Journal of Human Genetics|volume=80|pages=884–94|pmid=17436243|last2=Cadenas|first2=AM|last3=Regueiro|first3=M|last4=Singh|first4=NB|last5=Zhivotovsky|first5=LA|last6=Underhill|first6=PA|last7=Cavalli-Sforza|first7=LL|last8=Herrera|first8=RJ|issue=5|pmc=1852741}} |
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*{{cite book|url=https://books.google.com/books?id=V5oPGbeBnxkC|title=Ethnohistorical and Genetic Survey of Four Central Anatolian Settlements|isbn=978-0-549-80966-1|publisher=University of Pennsylvania|access-date=May 13, 2014|year=2008|first=Omer|last=Gokcumen}} |
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{{div col end}} |
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==External links== |
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{{Commons category|Haplogroup Q of Y-DNA}} |
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*[https://web.archive.org/web/20160308051230/https://genographic.nationalgeographic.com/?card=my045 Spread of Haplogroup Q], from [[The Genographic Project]], ''[[National Geographic (magazine)|National Geographic]]'' |
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*[http://www.familytreedna.com/public/india The India Genealogical DNA Project] |
*[http://www.familytreedna.com/public/india The India Genealogical DNA Project] |
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*[http://www.britishislesdna.com/ British Isles DNA Project] |
*[http://www.britishislesdna.com/ British Isles DNA Project] |
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{{DEFAULTSORT:Haplogroup Q-M242 (Y-Dna)}} |
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== References == |
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[[Category:Human Y-DNA haplogroups|Q-M242]] |
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===Citations=== |
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{{Reflist|colwidth=30em}} |
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=== Bibliography === |
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{{Div col|cols=2}} |
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*{{Cite journal | doi =10.1186/1471-2156-10-59 | title =Saudi Arabian Y-Chromosome diversity and its relationship with nearby regions | year =2009 | last1 =Abu-Amero | first1 =Khaled K | last2 =Hellani | first2 =Ali | last3 =González | first3 =Ana M | last4 =Larruga | first4 =Jose M | last5 =Cabrera | first5 =Vicente M | last6 =Underhill | first6 =Peter A | journal =BMC Genetics | volume =10 | pages =59 | pmid =19772609 | pmc =2759955 }} |
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*{{Cite journal | doi =10.1086/377588 | title =Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas | year =2003 | last1 =Bortolini | first1 =M | last2 =Salzano | first2 =F | last3 =Thomas | first3 =M | last4 =Stuart | first4 =S | last5 =Nasanen | first5 =S | last6 =Bau | first6 =C | last7 =Hutz | first7 =M | last8 =Layrisse | first8 =Z | last9 =Petzlerler | first9 =M | journal =The American Journal of Human Genetics | volume =73 | pages =524–39 | pmid =12900798 | issue =3 | pmc =1180678 }} |
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*{{Cite journal | doi =10.1038/sj.ejhg.5201934 | title =Y-chromosome diversity characterizes the Gulf of Oman | year =2007 | last1 =Cadenas | first1 =Alicia M | last2 =Zhivotovsky | first2 =Lev A | last3 =Cavalli-Sforza | first3 =Luca L | last4 =Underhill | first4 =Peter A | last5 =Herrera | first5 =Rene J | journal =European Journal of Human Genetics | volume =16 | pages =374–86 | pmid =17928816 | issue =3 }}*{{Cite journal | doi =10.1038/sj.ejhg.5201934 | title =Y-chromosome diversity characterizes the Gulf of Oman | year =2007 | last1 =Cadenas | first1 =Alicia M | last2 =Zhivotovsky | first2 =Lev A | last3 =Cavalli-Sforza | first3 =Luca L | last4 =Underhill | first4 =Peter A | last5 =Herrera | first5 =Rene J | journal =European Journal of Human Genetics | volume =16 | pages =374–86 | pmid =17928816 | issue =3 }} |
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*{{Cite journal | doi =10.1007/s00439-003-1031-4 | title =Excavating Y-chromosome haplotype strata in Anatolia | year =2004 | last1 =Cinnioglu | first1 =Cengiz | last2 =King | first2 =Roy | last3 =Kivisild | first3 =Toomas | last4 =Kalfoglu | first4 =Ersi | last5 =Atasoy | first5 =Sevil | last6 =Cavalleri | first6 =Gianpiero L. | last7 =Lillie | first7 =Anita S. | last8 =Roseman | first8 =Charles C. | last9 =Lin | first9 =Alice A. | journal =Human Genetics | volume =114 | pages =127–48 | pmid =14586639 | issue =2 }} |
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*{{Cite journal | doi =10.1038/sj.ejhg.5201726 | title =Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan | year =2006 | last1 =Firasat | first1 =Sadaf | last2 =Khaliq | first2 =Shagufta | last3 =Mohyuddin | first3 =Aisha | last4 =Papaioannou | first4 =Myrto | last5 =Tyler-Smith | first5 =Chris | last6 =Underhill | first6 =Peter A | last7 =Ayub | first7 =Qasim | journal =European Journal of Human Genetics | volume =15 | pages =121–6 | pmid =17047675 | issue =1 | pmc =2588664 }} |
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*{{Cite journal | doi =10.1086/516757 | title =The Himalayas as a Directional Barrier to Gene Flow | year =2007 | last1 =Gayden | first1 =T | journal =The American Journal of Human Genetics | volume =80 | pages =884–94 | pmid =17436243 | last2 =Cadenas | first2 =AM | last3 =Regueiro | first3 =M | last4 =Singh | first4 =NB | last5 =Zhivotovsky | first5 =LA | last6 =Underhill | first6 =PA | last7 =Cavalli-Sforza | first7 =LL | last8 =Herrera | first8 =RJ | issue =5 | pmc =1852741 }} |
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*{{Cite journal | doi =10.1007/s10038-005-0322-0 | title =Dual origins of the Japanese* common ground for hunter-gatherer and farmer Y chromosomes | year =2005 | last1 =Hammer | first1 =Michael F. | last2 =Karafet | first2 =Tatiana M. | last3 =Park | first3 =Hwayong | last4 =Omoto | first4 =Keiichi | last5 =Harihara | first5 =Shinji | last6 =Stoneking | first6 =Mark | last7 =Horai | first7 =Satoshi | journal =Journal of Human Genetics | volume =51 | pages =47–58 | pmid =16328082 | issue =1 }} |
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*{{Cite journal | doi =10.1038/ejhg.2009.6 | title =Y-Chromosome distribution within the geo-linguistic landscape of northwestern Russia | year =2009 | last1 =Mirabal | first1 =Sheyla | last2 =Regueiro | first2 =Maria | last3 =Cadenas | first3 =Alicia M | last4 =Cavalli-Sforza | first4 =L Luca | pmc =2986641 | last5 =Underhill | first5 =Peter A | last6 =Verbenko | first6 =Dmitry A | last7 =Limborska | first7 =Svetlana A | last8 =Herrera | first8 =Rene J | journal =European Journal of Human Genetics | volume =17 | pages =1260–73 | pmid =19259129 | issue =10 }} |
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*{{Cite journal | doi =10.1111/j.1469-1809.2006.00343.x | title =Y-chromosomal Binary Haplogroups in the Japanese Population and their Relationship to 16 Y-STR Polymorphisms | year =2007 | last1 =Nonaka | first1 =I. | last2 =Minaguchi | first2 =K. | last3 =Takezaki | first3 =N. | journal =Annals of Human Genetics | volume =71 | pages =480–95 | pmid =17274803 | issue =Pt 4 }} |
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*{{Cite journal | doi =10.1007/s00439-006-0213-2 | title =Investigating the effects of prehistoric migrations in Siberia* genetic variation and the origins of Yakuts | year =2006 | last1 =Pakendorf | first1 =Brigitte | last2 =Novgorodov | first2 =Innokentij N. | last3 =Osakovskij | first3 =Vladimir L. | last4 =Danilova | first4 =Al’Bina P. | last5 =Protod’jakonov | first5 =Artur P. | last6 =Stoneking | first6 =Mark | journal =Human Genetics | volume =120 | pages =334–53 | pmid =16845541 | issue =3 }} |
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*{{Cite journal | doi =10.1038/nature08835 | title =Ancient human genome sequence of an extinct Palaeo-Eskimo | year =2010 | last1 =Rasmussen | first1 =Morten | last2 =Li | first2 =Yingrui | last3 =Lindgreen | first3 =Stinus | last4 =Pedersen | first4 =Jakob Skou | last5 =Albrechtsen | first5 =Anders | last6 =Moltke | first6 =Ida | last7 =Metspalu | first7 =Mait | last8 =Metspalu | first8 =Ene | last9 =Kivisild | first9 =Toomas | journal =Nature | volume =463 | pages =757–62 | pmid =20148029 | issue =7282 }} |
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*{{Cite journal | doi =10.1159/000093774 | title =Iran* Tricontinental Nexus for Y-Chromosome Driven Migration | year =2006 | last1 =Regueiro | first1 =M. | last2 =Cadenas | first2 =A.M. | last3 =Gayden | first3 =T. | last4 =Underhill | first4 =P.A. | last5 =Herrera | first5 =R.J. | journal =Human Heredity | volume =61 | pages =132–43 | pmid =16770078 | issue =3 }} |
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*{{Cite journal | doi =10.1086/499411 | title =Polarity and Temporality of High-Resolution Y-Chromosome Distributions in India Identify Both Indigenous and Exogenous Expansions and Reveal Minor Genetic Influence of Central Asian Pastoralists | year =2006 | last1 =Sengupta | first1 =S | last2 =Zhivotovsky | first2 =L | last3 =King | first3 =R | last4 =Mehdi | first4 =S | last5 =Edmonds | first5 =C | last6 =Chow | first6 =C | last7 =Lin | first7 =A | last8 =Mitra | first8 =M | last9 =Sil | first9 =S | journal =The American Journal of Human Genetics | volume =78 | pages =202–21 | pmid =16400607 | issue =2 | pmc =1380230 }} |
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*{{Cite journal | doi =10.1186/1471-2148-7-232 | title =A novel subgroup Q5 of human Y-chromosomal haplogroup Q in India | year =2007 | last1 =Sharma | first1 =Swarkar | last2 =Rai | first2 =Ekta | last3 =Bhat | first3 =Audesh K | last4 =Bhanwer | first4 =Amarjit S | last5 =Bamezai | first5 =Rameshwar NK | journal =BMC Evolutionary Biology | volume =7 | pages =232 | pmid =18021436 | pmc =2258157 }} |
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*{{Cite journal | doi =10.1002/humu.20077 | title =Reconstruction of patrilineages and matrilineages of Samaritans and other Israeli populations from Y-Chromosome and mitochondrial DNA sequence Variation | year =2004 | last1 =Shen | first1 =Peidong | last2 =Lavi | first2 =Tal | last3 =Kivisild | first3 =Toomas | last4 =Chou | first4 =Vivian | last5 =Sengun | first5 =Deniz | last6 =Gefel | first6 =Dov | last7 =Shpirer | first7 =Issac | last8 =Woolf | first8 =Eilon | last9 =Hillel | first9 =Jossi | journal =Human Mutation | volume =24 | pages =248–60 | pmid =15300852 | issue =3 }} |
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*{{cite book| first= Spencer | last =Wells |title =The Journey of Man* A Genetic Odyssey|format =Digitised online by Google books|publisher=Random House|isbn= 0-8129-7146-9 }} |
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*{{Cite journal | doi =10.1038/nature02878 | title =Genetic evidence supports demic diffusion of Han culture | year =2004 | last1 =Wen | first1 =Bo | last2 =Li | first2 =Hui | last3 =Lu | first3 =Daru | last4 =Song | first4 =Xiufeng | last5 =Zhang | first5 =Feng | last6 =He | first6 =Yungang | last7 =Li | first7 =Feng | last8 =Gao | first8 =Yang | last9 =Mao | first9 =Xianyun | journal =Nature | volume =431 | pages =302–5 | pmid =15372031 | issue =7006 }} |
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*{{Cite journal | doi =10.1007/s004390000406 | title =Y chromosome haplotypes reveal prehistorical migrations to the Himalayas | year =2000 | last1 =Su | first1 =Bing | last2 =Xiao | first2 =Chunjie | last3 =Deka | first3 =Ranjan | last4 =Seielstad | first4 =Mark T. | last5 =Kangwanpong | first5 =Daoroong | last6 =Xiao | first6 =Junhua | last7 =Lu | first7 =Daru | last8 =Underhill | first8 =Peter | last9 =Cavalli-Sforza | first9 =Luca | journal =Human Genetics | volume =107 | pages =582–90 | pmid =11153912 | issue =6 }} |
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*{{Cite journal | doi =10.1016/j.ajhg.2008.01.020 | title =Y-Chromosomal Diversity in Lebanon Is Structured by Recent Historical Events | year =2008 | last1 =Zalloua | first1 =P | last2 =Xue | first2 =Y | last3 =Khalife | first3 =J | last4 =Makhoul | first4 =N | last5 =Debiane | first5 =L | last6 =Platt | first6 =D | last7 =Royyuru | first7 =A | last8 =Herrera | first8 =R | last9 =Hernanz | first9 =D | journal =The American Journal of Human Genetics | volume =82 | pages =873–82 | pmid =18374297 | issue =4 | pmc =2427286 }} |
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*{{Cite journal | doi =10.1093/molbev/msh009 | title =High-Resolution SNPs and Microsatellite Haplotypes Point to a Single, Recent Entry of Native American Y Chromosomes into the Americas | year =2003 | last1 =Zegura | first1 =S. L. | journal =Molecular Biology and Evolution | volume =21 | pages =164–75 | pmid =14595095 | last2 =Karafet | first2 =TM | last3 =Zhivotovsky | first3 =LA | last4 =Hammer | first4 =MF | issue =1 }} |
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*{{Cite book | isbn =978-0-549-80966-1 }} |
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</div> |
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{{DEFAULTSORT:Haplogroup Q (Y-Dna)}} |
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[[Category:Human Y-DNA haplogroups|Q]] |
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[[Category:Natural history of the Americas]] |
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[[ca:Haplogrup Q del cromosoma Y humà]] |
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[[fr:Haplogroupe Q (Y-ADN)]] |
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[[hi:पितृवंश समूह क्यु]] |
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[[ru:Гаплогруппа Q (Y-ДНК)]] |
Latest revision as of 19:55, 1 January 2025
Haplogroup Q | |
---|---|
Possible time of origin | 17,200 to 31,700 years ago[2][3][4] (approximately 24,500 years BP) |
Possible place of origin | Central Asia,[5][6] South Central Siberia[3] |
Ancestor | P1-M45 |
Descendants | Q1 (L232/S432) |
Defining mutations | M242 rs8179021 |
Highest frequencies | Kets 93.8%,[7] Indigenous peoples of South America 92%,[8] Inuit 80%,[9] Turkmens from Karakalpakstan (mainly Yomut) 73%,[10] Selkups 66.4%.,[7] Altaians 63.6%.,[11] Tuvans (from Xinjiang) 62.5%.,[12] Chelkans 60.0%.,[11] Greenlandic Inuit 54%,[13] Tubalar 41%,[11] Siberian Tatars (Ishtyak-Tokuz Tatars) 38%,[14] the indigenous peoples of the Americas, Akha people of northern Thailand, Mon-Khmer people, some tribes of Assam and Swati tribe of Pakistan |
Haplogroup Q or Q-M242 is a Y-chromosome DNA haplogroup. It has one primary subclade, Haplogroup Q1 (L232/S432), which includes numerous subclades that have been sampled and identified in males among modern populations.
Q-M242 is the predominant Y-DNA haplogroup among Native Americans, Swati tribe and several peoples of Central Asia and Northern Siberia.
Origins
[edit]Haplogroup Q-M242 is one of the two branches of P-P226 (M45), the other being R-M207.[15]
Q-M242 is believed to have arisen around the Altai Mountains area (or South Central Siberia),[3] approximately 17,000[3] to 31,700 years ago.[4] However, the matter remains unclear due to limited sample sizes and changing definitions of Haplogroup Q: early definitions used a combination of the SNPs M242, P36.2, and MEH2 as defining mutations.
Technical specification of mutation
[edit]The polymorphism, "M242", is a C→T transition residing in intron 1 (IVS-866) of the DBY gene and was discovered by Mark Seielstad et al. in 2003.[16] The technical details of M242 are:
- Nucleotide change: C to T
- Position (base pair): 180
- Total size (base pairs): 366
- Forward 5′→ 3′: aactcttgataaaccgtgctg
- Reverse 5′→ 3′: tccaatctcaattcatgcctc
Subclades
[edit]In Y chromosome phylogenetics, subclades are the branches of a haplogroup. These subclades are also defined by single-nucleotide polymorphisms (SNPs) or unique-event polymorphisms (UEPs). Haplogroup Q-M242, according to the most recent available phylogenetics has between 15 and 21 subclades. The scientific understanding of these subclades has changed rapidly. Many key SNPs and corresponding subclades were unknown to researchers at the time of publication are excluded from even recent research. This makes understanding the meaning of individual migration paths challenging.
Phylogenetic trees
[edit]There are several confirmed and proposed phylogenetic trees available for haplogroup Q-M242. The scientifically accepted one is the Y Chromosome Consortium (YCC) one published in Karafet 2008 and subsequently updated. A draft tree that shows emerging science is provided by Thomas Krahn at the Genomic Research Center in Houston, Texas. The International Society of Genetic Genealogy (ISOGG) also provides an amateur tree.
The 2015 ISOGG tree
[edit]The subclades of Haplogroup Q-M242 with their defining mutation (s), according to the 2015 ISOGG tree[5] are provided below. The first three levels of subclades are shown. Additional detail is provided on the linked branch article pages.
- Q-M242 M242
The Genomic Research Center draft tree
[edit]Below is a 2012 tree by Thomas Krahn of the Genomic Research Center.[17] The first three levels of subclades are shown. Additional detail is provided on the linked branch article pages.[18]
The Y Chromosome Consortium tree
[edit]This is the 2008 tree produced by the Y Chromosome Consortium (YCC).[19] Subsequent updates have been quarterly and biannual. The current version is a revision of the 2010 update.[20] The first three levels of subclades are shown. Additional detail is provided on the linked branch article pages.
Phylogenetic variants
[edit]The subclade (under Q-MEH2) proposed by Sharma (2007), which shows polymorphism (ss4bp, rs41352448) at 72,314 position of human arylsulfatase D pseudogene, is not represented in any current trees under Q-MEH2.[21] The most plausible explanation for this could be an ancestral migration of individuals bearing Q-MEH2 to the Indian subcontinent followed by an autochthonous differentiation to Q-ss4bp.[6]
Distribution
[edit]Americas
[edit]Several branches of haplogroup Q-M242 have been predominant pre-Columbian male lineages in indigenous peoples of the Americas. Most of them are descendants of the major founding groups who migrated from Asia into the Americas by crossing the Bering Strait.[3] These small groups of founders must have included men from the Q-M346, Q-L54, Q-Z780, and Q-M3 lineages. In North America, two other Q-lineages also have been found. These are Q-P89.1 (under Q-MEH2) and Q-NWT01. They may have not been from the Beringia Crossings but instead come from later immigrants who traveled along the shoreline of Far East Asia and then the Americas using boats.
It is unclear whether the current frequency of Q-M242 lineages represents their frequency at the time of immigration or is the result of the shifts in a small founder population over time. Regardless, Q-M242 came to dominate the paternal lineages in the Americas.
North America
[edit]In the indigenous people of North America, Q-M242 is found in Na-Dené speakers at an average rate of 68%. The highest frequency is 92.3% in Navajo, followed by 78.1% in Apache,[3] 87%[3] in SC Apache,[22] and about 80% in North American Eskimo (Inuit, Yupik)–Aleut populations. (Q-M3 occupies 46% among Q in North America)[23]
On the other hand, a 4000-year-old Saqqaq individual belonging to Q1a-MEH2* has been found in Greenland. Surprisingly, he turned out to be genetically more closely related to Far East Siberians such as Koryaks and Chukchi people rather than Native Americans.[24] Today, the frequency of Q runs at 53.7% (122/227: 70 Q-NWT01, 52 Q-M3) in Greenland, showing the highest in east Sermersooq at 82% and the lowest in Qeqqata at 30%.[13]
Q-M242 is estimated to occupy 3.1% of the whole US population in 2010:[25]
Ethnicity | Percentage of USA population † | Haplogroup Q frequency |
---|---|---|
White | 63.7% | Q-P36* 0.6% & Q-M3 0.1% |
Hispanic | 16.3% | Q-P36* 3.8% & Q-M3 7.9% |
Black | 12.6% | Q-P36* (xM3) 0.2% |
Asian | 4.8% | ~0% |
Native American ‡ | 0.9% | Q-P36* 31.2% & Q-M3 26.9% |
Source :[25]
† According to the US National Population Census data (2010)[26] ‡ Mainland and Alaska, not including the Pacific islands |
Mesoamerica & South America
[edit]Haplogroup Q-M242 has been found in approximately 94% of Indigenous peoples of Mesoamerica and South America.[8]
The frequencies of Q among the whole male population of each country reach as follows:
- 61% in Bolivia.[27]
- 51% in Guatemala,[28]
- 40.1% (159/397)[29] to 50% in Peru
- 37.6% in Ecuador,[30]
- 37.3% (181/485) in Mexico[29] (30.8% (203/659) among the specifically Mestizo segment)[31]
- 31.2% (50/160) in El Salvador,[32]
- 15.3% (37/242) to 21.8% (89/408) in Panama,[29][33]
- 16.1% in Colombia,[34]
- 15.2% (25/165) in Nicaragua,[35]
- 9.7% (20/206) in Chile,[29]
- 5.3% (13/246 in 8 provinces in northeastern, central, southern regions)[36] to 23.4% (181/775 in 8 provinces in central-west, central, northwest regions)[37] in Argentina,
- 5% in Costa Rica,[38]
- 3.95% in Brazil,[39] and so on.
Asia
[edit]Q-M242 originated in Asia (Altai region), and is widely distributed across it.[3] Q-M242 is found in Russia, Siberia (Kets,[7] Selkups, Siberian Yupik people, Nivkhs, Chukchi people,[40] Yukaghirs, Tuvans,[41] Altai people,[11] Koryaks, etc.), Mongolia,[42] China,[43][44] Uyghurs,[42] Tibet,[45] Korea, Japan, Indonesia,[46] Vietnam,[47] Thailand,[48] India,[49] Pakistan,[49] Afghanistan, Iran,[50] Iraq, Saudi Arabia, Turkmenistan, Uzbekistan, and so on. (For details, see below.)
North Asia
[edit]In Siberia, the regions between Altai and Lake Baikal, which are famous for many prehistoric cultures and as the most likely birthplace of haplogroup Q, exhibit high frequencies of Q-M242. In a study (Dulik 2012),[51] Q-M242 (mostly Q-M346 including some Q-M3) has been found in 24.3% (46/189: 45 Q-M346, 1 Q-M25) of all Altaian samples. Among them, Chelkans show the highest frequency at 60.0% (15/25: all Q-M346), followed by Tubalars at 41% (11/27: 1 Q-M25, 10 Q-M346) and Altaians-Kizhi at 17% (20/120). In a former study, Q-M242 is found in 4.2% of southern Altaians and 32.0% of northern Altaians with the highest frequency of 63.6% in Kurmach-Baigol (Baygol). The frequency reaches 13.7% (20/146) in the whole samples.[11] In another study,[52] the frequency rises up to 25.8% (23/89: all Q-M346) in Altaians. Based on the results of these studies, the average frequency of Q-M242 in Altaians is about 21%.
Tuva, which is located on the east side of Altai Republic and west of Lake Baikal as well as on the north side of Mongolia, shows higher frequency of Q-M242. It is found in 14%[53]~38.0% (41/108)[52] of Tuvans. Also, Todjins (Tozhu Tuvans) in eastern Tuva show the frequency at ≤22.2% (8/36 P(xR1)[54])~38.5% (10/26, all Q-M346(xM3)).[52] So, the average frequency of Q-M242 among Tuvans-Todjins in Tuva Republic is about 25%. Haplogroup Q-M242 has been found in 5.9% (3/51) of a sample of Tuvans from the village of Kanasi, 9.8% (5/51) of a sample of Tuvans from the village of Hemu, and 62.5% (30/48) of a sample of Tuvans from the village of Baihaba in northern Xinjiang near the international border with Altai Republic.[12]
In Siberian Tatars, the Ishtyako-Tokuz sub-group of Tobol-Irtysh group has a frequency of Q-M242 at 38%.[14]
The highest frequencies of Q-M242 in Eurasia are witnessed in Kets (central Siberia) at 93.8% (45/48) and in Selkups (north Siberia) at 66.4% (87/131).[7] Russian ethnographers believe that their ancient places were farther south, in the area of the Altai and Sayan Mountains[3] (Altai-Sayan region). Their populations are currently small in number, being just under 1,500 and 5,000 respectively. In linguistic anthropology, the Ket language is significant as it is currently the only surviving one in the Yeniseian language family which has been linked by some scholars to the Native American Na-Dené languages[55] and, more controversially, the language of the Huns. (See: L. Lieti, E. Pulleybank,[56] E. Vajda,[57] A. Vovin,[58] etc.) Q-M346 is also found at lower rates in Sojots (7.1%, Q-M346), Khakassians (6.3%, Q-M346), Kalmyks (3.4%, Q-M25, Q-M346)[52] and Khanty,[59] and so on.
In far eastern Siberia, Q-M242 is found in 35.3% of Nivkhs (Gilyaks) in the lower Amur River, and 33.3% of Chukchi people and 39.2% of Siberian Yupik people in Chukotka (Chukchi Peninsula).[40] It is found in 30.8% of Yukaghirs who live in the basin of the Kolyma River, which is located northwest of Kamchatka.[41] It is also found in 15% (Q1a* 9%, Q-M3 6%) of Koryaks in Kamchatka.[29]
East Asia
[edit]In some studies, various subgroups of Q-M242 are observed in Mongolia. Q1a2-M346 (mostly Q-L330) occupies 1.4[29]~3.1%[50] of Mongols (1/2~2/3 among Q samples), followed by Q1a1a1-M120 (0.25[29]~1.25%[50]), Q1a1b-M25 (0.25[29]~0.63%[50]), Q1b-M378. In another study, Q is found in 4% of Mongols.[8] Karafet et al. (2018) found Q-L54(xM3) in 2.7% (2/75) and Q-M25 in another 2.7% (2/75) for a total of 5.3% (4/75) haplogroup Q Y-DNA in a sample of Khalkha Mongols from Ulaanbaatar, Mongolia.[60] Based on these studies, the average frequency of Q-M242 in Mongols is estimated to be about 4~5%.
However, most of Q-M242 people in East Asia belong to subclade Q-M120, which distributes most intensively across northern China (the provinces of which the capitals locate northern to Huai River-Qin Mountains line). Q-M242 ranged from 4~8% in northwest China (Xinjiang, Gansu, Shaanxi), north China (Shanxi, Hebei), central China (Henan), and upper east China (Shandong) to 3~4% in northeast China. The average frequency of Q-M242 in northern China is around 4.5%. However, it decreases to about 2% in southern China.[43][44] In a study published in 2011, researchers have found Q-M242 in 3.3% (12/361) of the samples of unrelated Han-Chinese male volunteers at Fudan University in Shanghai with the origins from all over China, though with the majority coming from east China.[61] In another study published in 2011, Hua Zhong et al. found haplogroup Q-M242 in 3.99% (34/853, including 30/853 Q-M120, 3/853 Q-M346, and 1/853 Q-M25) of a pool of samples of Han Chinese from northern China and 1.71% (15/876, including 14/876 Q-M120 and 1/876 Q-M346) of a pool of samples of Han Chinese from southern China.[62] Q1a1-M120 is unique to East Asians. It is not found in South east Asia except with low diversity in Y-STR among southern Han Chinese indicating it spread during the Neolithic with Han Chinese culture to southern China from northern China. Q1a3*-M346 is only found among Hui and southern Han Chinese in South East Asia in southern China but not found in non-Han indigenous peoples at all. It came from northern China (north east Asia) with the Han. Only Native Americans have Q1a3a-M3, which is a descendant haplogroup of Q1a3*-M346. The Americas was populated by migrants from Central Asia in prehistoric times.[63] Q1a1 is attested in over 3,000 year old Han Chinese ancestral remains in the Shang and Zhou dynasties from the Hengbei archeological site.[64] Modern northern Han Chinese Y haplogroups and mtdna match those of ancient northern Han Chinese ancestors 3,000 years ago from the Hengbei archeological site. 89 ancient samples were taken. Y haplogroups O3a, O3a3, M, O2a, Q1a1, and O* were all found in Hengbei samples.[65]
Q-M242 has been found with notable frequency in some samples of Uyghurs: 15.38% (22/143, including 6/143 Q-M378, 5/143 Q-P36.2*, 4/143 Q-M120, 4/143 Q-M346, 1/143 Q-M25) of a sample of Uyghurs from the Turpan area (吐鲁番地区),[66] 7.9% (6/76, including 2/76 Q1b1-L215/Page82/S325, 1/76 Q1a2-M346*, 1/76 Q1a1a1-M120, 1/76 Q1a2a1c-L330*, 1/76 Q1a2a1c1-L332) of a sample of Dolan Uyghurs (刀郎人) from Horiqol Township of Awat County,[67] and 7.74% (37/478, including 24/478 Q-M346, 7/478 Q-P36.2*, 5/478 Q-M120) of a sample of Uyghurs from the Hotan area (和田地区).[68] However, other studies have found haplogroup Q in much smaller percentages of Uyghur samples: 3.0% (2/67) Q-P36 Uygur,[69] 1.6% (1/64) Q-M120 Lop Uyghur (罗布人).[67] Haplogroup Q was not observed in a sample of 39 Keriyan Uyghurs (克里雅人) from the village of Darya Boyi, located on the Keriya River deep in the Taklamakan Desert.[67]
Haplogroup Q was observed in 3.2% (5/156 : 2 Q-M120, 3 Q-M346) of males in Tibet in one study[45] and in 1.23% (29/2354) of males in Tibet in another study,[70] but this haplogroup was not observed in a sample of males from Tibet (n=105) in a third study.[69]
It is found in about 1.9% of South Koreans,[71][72][73] showing the highest frequency in Seoul and Gyeonggi Province at 2.7% and decreasing ones to the south (Kim 2010). It has been found in about 0.3% of Japanese[74][69][75][76][77] (with known examples from Shizuoka[69] and Saitama[76]) and in 0.3%[48]~1.2%[78] of Taiwanese.
Subclade Q1b-M378 is also found in China and its neighboring countries at very low frequencies. It exists throughout all Mongolia, with rare examples in Japan.[79]
Southeast Asia
[edit]Haplogroup Q shows low frequencies in Southeast Asia. In a study,[46] the frequencies of haplogroup Q is 5.4% (2/37) in Indonesia, 3.1% (2/64) in the Philippines, 2.5% (1/40) in Thailand. However, other studies show 0% or near 0% frequencies in those countries.[48]
In the case of Vietnam, the frequency is 7.1% in one study of a sample of Vietnamese reported to be from southern Vietnam[80][81] and 4.3% in a sample of Kinh people from Ho Chi Minh City in southern Vietnam,[77] but 0% or under 1% in other studies in which samples have been collected in Hanoi in northern Vietnam.[46][81][48] So, it is hard to define average frequencies. However, Macholdt et al. (2020) have tested a sample of fifty Kinh people from northern Vietnam (all but one of whom are from the Red River Delta region, and 42 of whom are from Hanoi) and found that two of them (4%) belong to Q-M120.[82]
Only some regions and ethnic groups in the continent show high frequencies. Q-M242 is found in 2.8% (3/106, all Q-M346) in Myanmar, and all the Q samples are concentrated in 18.8% in Ayeyarwady (2/11) and 7.1% Bago (1/14) regions in southwest Myanmar.[83] And, Q-M242 is found in 55.6% (15/27) in the Akha tribe in northern Thailand.[48]
Central Asia
[edit]In Central Asia, the southern regions show higher frequencies of Q than the northern ones.
In the northern regions, Q-M242 is found in about 2%[84]~6%[85][86] (average 4%) of Kazakhs. A study published in 2017 found haplogroup Q Y-DNA in 3.17% (41/1294) of a large pool of samples of Kazakh tribes; however, haplogroup Q was concentrated in the members of the Qangly tribe (27/40 = 67.5%), and it was much less common among the other tribes.[87] The Qangly tribe is related at least in name to the earlier Kankalis and probably also the Kangar union. Haplogroup Q is found in about 2% of Kyrgyz people.[50][85][86]
In the southern regions, Q-M242 is found in 5%[88]~6%[85][86] of Tajiks (Tajikistan). Karafet et al. 2001 found P-DYS257(xQ1b1a1a-M3, R-UTY2), which should be roughly equivalent to haplogroup Q-M242(xM3), in 4/54 = 7.4% of a sample of Uzbeks, apparently sampled in Uzbekistan.[89] Wells et al. 2001 found P-M45(xM120, M124, M3, M173), which should be roughly equivalent to a mix of Q-M242(xM120, M3) and R2-M479(xR2a-M124), in 20/366 = 5.5% of a pool of samples of Uzbeks from seven different regions of Uzbekistan.[85] Di Cristofaro et al. 2013 found Q-M242 in 11/127 = 8.7% of a pool of samples of Uzbeks from three different provinces of Afghanistan, including 5/94 Q-M242(xM120, M25, M346, M378), 4/94 Q-M346, and 1/94 Q-M25 (10/94 = 10.6% Q-M242 total) in a sample of Uzbeks from Jawzjan Province, whose northern border abuts the southeastern corner of Turkmenistan, and 1/28 Q-M242(xM120, M25, M346, M378) in a sample of Uzbeks from Sar-e Pol Province.[50] Wells et al. (2001) found P-M45(xM120, M124, M3, M173) in 10.0% (3/30) of a sample of Turkmens from Turkmenistan, whereas Karafet et al. (2018) found Q-M25 in 50.0% (22/44) of another sample of Turkmens from Turkmenistan, so the frequency of haplogroup Q in that country is not yet clear. However, Grugni et al. (2012) found Q-M242 in 42.6% (29/68) of a sample of Turkmens from Golestan, Iran, and Di Cristofaro et al. (2013) found Q-M25 in 31.1% (23/74) and Q-M346 in 2.7% (2/74) for a total of 33.8% (25/74) Q-M242 in a sample of Turkmens from Jawzjan, Afghanistan, so the frequency of Q-M242 may reach about 40% in Turkmens of Afghanistan and Iran who live in the areas adjacent to Turkmenistan.
Q-M242 accounts for 6.9% of Afghans in a study (Haber 2012). In another study (Cristofaro 2013) with a larger sampling, the frequency of Q rises to 8.9% (45/507). Haplogroup Q occurs at a frequency of 8% (11/136) in Afghan Pashtuns and 3% (5/142) in Afghan Tajiks.[90][91] In this study(Cristofaro 2013), Turkmens of Jowzjan Province which is neighboring to Turkmenistan show the highest frequency at 33.8% (25/74: 23 Q-M25, 2 Q-M346), followed by Uzbeks at 8.7% (11/144: 6 Q*, 1 Q-M25, 4 Q-M346).[50]
Southwest Asia
[edit]Southwest Asia exhibits high frequencies of Q in northern Iran, and gradually lowering ones to the southwest.
Q-M242 accounts for 5.5% (52/938) in Iran according to Grugni 2012, which shows a large and well allocated sampling. The Q samples (52) in the study consist of various subclades such as Q* (3), Q-M120 (1), Q-M25 (30), Q-M346 (8), Q-M378 (10). The highest frequency is at 42.6% (29/68, all Q-M25) in Turkmens of Golestan, followed by 9.1% in Isfahan (Persian people), 6.8% in Khorasan (Persian people), 6% in Lorestan (Luristan, Lurs), 4.9% in Azarbaijan Gharbi (5.1% of Assyrians and 4.8% of Azeris), 4.5% in Fars (Persian people), and so on.[92] Turkmens are known as the descendants of Oghuz Turks who built many Turkic empires and dynasties. Other studies also show similar frequencies.[93][94][95]
In a study (Zahery 2011), the frequency of Q is 1.9% (3/154: all Q-M378) in Iraqis (x Marsh Arabs), and 2.8% (4/143: 1 Q-M25, 3 Q-M378) in Marsh Arabs who are known as the descendants of ancient Sumerians.[96]
Approximately 2.5% (4/157: 3 Q*, 1 Q-M346) of males in Saudi Arabia belong to haplogroup Q. It also accounts for 1.8% (3/164: 2 Q*, 1 Q-M346) in the United Arab Emirates and 0.8% (1/121: Q*) in Oman peoples.[97][98]
Haplogroup Q-M242 has also been found in 1.1% (1/87, Q-P36) Syrians[80] and 2.0% (18/914, 14 Q*, 4 Q-M25) in Lebanese.[99]
Approximately 2% (10/523: 9 Q*, 1 Q-M25) of males in Turkey belong to haplogroup Q.[100] In a study (Gokcumen 2008), it was found that among Turks who belong to the Afshar tribe (one of Oghuz Turks) haplogroup Q-M242 is seen with a prevalence of 13%.[101]
South Asia
[edit]In Pakistan at the eastern end of the Iranian Plateau, the frequency of haplogroup Q-M242 is about 2.2% (14/638)[102]~3.4% (6/176).[103]
In a study (Sharma2007), Q-M242 is observed in 2.38% (15/630) of Indian people belonging to different regions and social categories. What is interesting is 14/15 samples do not belong to any known subgroups of Q-M242, with 4 among them showing novel (Indian-specific) 'ss4bp' allele under Q-MEH2. This study also reflects the results of some former studies (Sengupta 2006, Seielstad 2003). And, the accumulated result (frequency) of 3 studies is turned out to be 1.3% (21/1615), with 11 out of 21 Q samples.[6] (For more information, see Y-DNA haplogroups in populations of South Asia)
In a regional study in Gujarat (Western India), Q-M242 was found at its highest 12% (3/25) among Nana Chaudharis while the overall percentage in Gujarat was found to be 2.8% (8/284).[104] In another study, 2.6% of Tharus in Chitwan district and 6.1% (3/49) of Hindus in New Delhi, the capital of India were found to be Q-M242 positive.[105]
In a study in which Q-M242 is just classified in P* group, P* (x R1, R2) accounts for 9.7% (23/237: Chakma 13/89, Marma 4/60, Tripura 6/88) in three ethnic groups of Bangladesh.[106] In many cases, all or most of P* (x R1, R2) means Q-M242, and thus most of P* (9.7%) samples in that study can be estimated to be Q-M242.
1.2% of Nepalese people in Kathmandu, the capital of Nepal and 3.2% of people from Tibet are in Q-M242.[45]
3.3% of Sri Lankans[80] are also in Q-M242.
Europe
[edit]Q-M242 is distributed across most European countries at low frequencies, and the frequencies decrease to the west and to the south.
Central- and Eastern Europe
[edit]In Central- Eastern Europe, Q-M242 comprises about 1.7% of males. Q-M242 is found in about 2% of Russians,[107] 1.5% of Belarusians,[108] 1.3% of Ukrainians[citation needed] 1.3% of Poles (Poland),[109] 2% of Czechs,[110] 1.5% of Slovaks,[111] about 2.2% of Hungarians,{citation needed} 1.2% of Romanians,[112] 0.8% of Moldovans,[113] and 0.5% (4/808: 2 Q-M378, 1 Q-M346, 1 Q-M25) of Bulgarians[114] On the other hand, 3.1% of Székelys from Transylvania (who have claimed to be descendants of Attila's Huns) turned out to be P* (xR1-M173),[115] which virtually means Q-M242. In a related DNA Project of FT-DNA, the frequency of Q-M25 in Székelys (Szeklers) reaches 4.3%.[116][117]
The Caucasus region shows a frequency at 1.2% in a study,[94] but it may reach over 4% in Azerbaijan, in that 4.9% of the neighboring Iranian Azerbaijanis harbor Q-M242.[93] It is 1.3% in Georgians and Armenians respectively, and Armenian subclades consist of Q-M378 (L245), Q-M346, and Q-M25.[118]
Northern Europe
[edit]In Northern Europe, haplogroup Q comprises about 2.5% of males. According to the Swedish Haplogroup Database, 4.1% (27/664, as of Jan 2016) of Swedish males belong to Q-M242. About 2/3 of the samples analyzed subclades in detail belong to Q1a2b-F1161/L527 and about 1/3 are in Q1a2a-L804. By county, they are distributed intensively in the southern region (Götaland,: not to be confused with Gotland), and rarely to the north. If recalculated by county-population weights, the frequency of Q in Sweden reaches 4.7%.
In Norway, Q-M242 is found in about 2.6% (~4%[119]) of males, with Q-L804 being more common than Q-F1161/L527.[120] It is observed among 1.6% of males in Denmark, 3% in the Faroe Islands (known to be related to Vikings).[121] In an article (Helgason et al.) on the haplotypes of Icelanders, 7.2% (13/181) of males in Iceland are labelled as R1b-Branch A, but they are actually Q-M242.[119][122] On the other hand, it is 0.2% in Finland,[123] 4.6% in Latvia,[124] 1.1% in Lithuania,[125] 0.5% in Estonia.
Western Europe
[edit]In Western Europe, Q-M242 is observed at very low frequencies, around 0.5% in most of the countries, such as Germany, France, United Kingdom, etc., but some regions show a little higher. It is 2.1% in Switzerland,[126] and it reaches 5.1% in Lyon (Rhône-Alpes) region of France.[127] It is about 4% in Shetland of northernmost Britain, with a place in it showing the highest figure at 8%. Shetland has been known to be a settlement of Vikings. And, surprisingly, Q-M242 in Shetland (also in some areas of Scandinavia, Faroe Islands, Iceland, and the United Kingdom) has turned out to be generically closely linked to the Q-M242 in Central Asia. Also, Shetland (Norse) Q-M242 is revealed to be linked to some Q-M242 of Azeris (Azerbaijan).[119]
Southern Europe
[edit]Southern Europe also shows low frequencies of Q around 0.5%~1%, but some regions exhibits different figures. It is 1.9% in mainland Croatia, but it reaches 14.3% (13/91) in Hvar Islands and 6.1% (8/132) in Korčula.[127] Also, it is about 0.6% in Italy, but it rises to 2.5% (6/236) in Sicily, where it reaches 16.7% (3/18) in Mazara del Vallo region, followed by 7.1% (2/28) in Ragusa, 3.6% in Sciacca,[128] and 3.7% in Belvedere Marittimo.[129]
On the other hand, according to a study (Behar 2004), 5.2% (23/441) of Ashkenazi Jewish males belong to haplogroup Q-P36.[130] This has subsequently been found to be entirely the Q-M378 subclade and may be restricted to Q-L245. Also, 2.3% (4/174)[131]~5.6% (3/53)[132] of Sephardi Jews are in haplogroup Q.
Africa
[edit]Haplogroup Q is rarely found across North Africa. It is observed in 0.7% (1/147),[98] of Egyptians and in 0.6% (1/156)[94] of Algerian people. Surprisingly, it is also witnessed in 0.8% (3/381, all Q-M346) of males from Comoros which is located in between East Africa and Madagascar.
To combine the data above, Q-M242 is estimated to be in about 3.1% of males of the world.
Subclade distribution
[edit]- Q (M242)
- Q* – Found with low frequency in India and Pakistan.[49] Important in Afghanistan, paragroup Q-M242 (xMEH2, xM378) was found in eight Pashtun males (3 Kabul, 4 Laghman, 1 Kapisa).[133] Also found in one Rapanui male of Easter Island.[134]
- Q-P36.2 (P36.2) Found with low frequency in Iran.[135]
- Q-MEH2 (MEH2) Was found in Koryaks (at 10.3%), although the level of STR diversity associated with Q-MEH2 is very low, this lineage appears to be closest to the extinct Paleo-Eskimo individuals belonging to the Saqqaq culture arisen in the New World Arctic about 5.5 Ka.[136]
- Q-M120 (M120, M265/N14) – It has been found at low frequency among Han Chinese,[43][44] Dungans,[85] Nivkhs,[137] Koryaks,[137] Yukaghirs,[137] Vietnamese,[77][82] Japanese,[76] Tuvans,[138] Kalmyks,[139] Koreans,[85] Mongols in Mongolia,[140] Tibetans,[44][45][78] and Hmong Daw in Laos.[141] It also has been reported in samples of Bhutanese,[142] Hazara,[103] Bruneian Murut,[143] Gujar,[6] Baloch,[92] Georgian,[144] and Peruvian[77] populations.
- Q-M25 (M25, M143) – Found with high frequency of 30-45% in Turkmens and Turkmenistan Confused with R1b1 because of P25. Found with high frequency in Turkmens of Golestan province (Iran),[92] Jawzjan ( Afghanistan),[140] and with low to moderate frequency in Lebanon,[145] Mongolia,[140] and Turkey[100]
- Q-M346 (L56, L57, M346) – Found at low frequency in Europe, South Asia and West Asia. It has been found in Pakistan,[103] Iran,[140] Afghanistan,[140] Kyrgyzstan,[140] Saudi Arabia,[98] the United Arab Emirates,[97] India,[103] Mongolia,[140] Tibet,[45] and Bali.[47]
- Q-L53 (L53, L54, L55, L213)
- Q-M3 (M3) – Common in indigenous peoples of the Americas[146]
- Q-M19 (M19) – Found among some indigenous peoples of South America, such as the Ticuna and the Wayuu[8]
- Q-M194 (M194) – In South America
- Q-M199 (M199, P106, P292) – In South America
- Q-M3 (M3) – Common in indigenous peoples of the Americas[146]
- Q-M323 (M323) – It has been detected in Yemenite Jews.[147]
- Q-L53 (L53, L54, L55, L213)
- Q-L275 (L275, L314)
- Q-M378 (M378) – It is widely distributed in Europe, South Asia, West and East Asia. It is found among samples of Hazaras and Sindhis.[103] It is also found in the Mongols, the Japanese people and the Uyghurs of North-Western China in two separate groups.[148] The Q-M378 subclade is a branch to which Q-M242 men in some European Jewish Diaspora populations belong. Its subbranch Q-L245's subclades Q-Y2200 and Q-YP1035 are found in Ashkenazi Jews.[149] Some Sephardic Jews carry other subclades of Q-L245, including Q-BZ3900, Q-YP745, and Q-YP1237. Q-M378 samples also have been located in Central America (Panama) and South America (Andean Region)[29]
- Q-MEH2 (MEH2) Was found in Koryaks (at 10.3%), although the level of STR diversity associated with Q-MEH2 is very low, this lineage appears to be closest to the extinct Paleo-Eskimo individuals belonging to the Saqqaq culture arisen in the New World Arctic about 5.5 Ka.[136]
Y-DNA Q samples from ancient sites
[edit]- South Central Siberia (near Altai)
- Afontova-Gora-2, Yenisei River Bank, Krasnoyarsk (South Central Siberia of Russia), 17000YBP: Q1a1-F1215 (mtDNA R)[150]
- North America
- Anzick-1, Clovis culture, western Montana, 12600YBP: Q1a2-L54* (not M3, mtDNA D4h3a)[151][152]
- Kennewick Man, Washington, 8500YBP: Q1a2-M3 (mtDNA X2a)[153]
- Altai (West Mongolia)
- Greenland
- Saqqaq (Qilakitsoq), Greenland, 4000YBP: Q1a-YP1500[155] (mtDNA D2a1)[24]
- China
- Hengbei site (Peng kingdom cemetery of Western Zhou period), Jiang County, Shanxi, 2800-3000YBP: 9 Q1a1-M120, 2 O2a-M95, 1 N, 4 O3a2-P201, 2 O3, 4 O*[156]
- In another paper, the social status of those human remains of ancient Peng kingdom(倗国) are analyzed. aristocrats: 3 Q1a1 (prostrate 2, supine 1), 2 O3a (supine 2), 1 N (prostrate) / commoners : 8 Q1a1 (prostrate 4, supine 4), 3 O3a (prostrate 1, supine 2), 3 O* (supine 3) / slaves: 3 O3a, 2 O2a, 1 O*[157]
- (cf) Pengbo (倗伯), Monarch of Peng Kingdom is estimated as Q-M120.
- Pengyang County, Ningxia, 2500YBP: all 4 Q1a1-M120[156] (with a lot of animal bones and bronze swords and other weapons, etc.)
- Heigouliang, Xinjiang, 2200YBP: 6 Q1a* (not Q1a1-M120, not Q1a1b-M25, not Q1a2-M3), 4 Q1b-M378, 2 Q* (not Q1a, not Q1b: unable to determine subclades):[158]
- In a paper (Lihongjie 2012), the author analyzed the Y-DNAs of the ancient male samples from the 2nd or 1st century BCE cemetery at Heigouliang in Xinjiang – which is also believed to be the site of a summer palace for Xiongnu kings – which is east of the Barkol basin and near the city of Hami. The Y-DNA of 12 men excavated from the site belonged to Q-MEH2 (Q1a) or Q-M378 (Q1b). The Q-M378 men among them were regarded as hosts of the tombs; half of the Q-MEH2 men appeared to be hosts and the other half as sacrificial victims.
- Xiongnu site in Barkol, Xinjiang, all 3 Q-M3
- In L. L. Kang et al. (2013), three samples from a Xiongnu) site in Barkol, Xinjiang were found to be Q-M3 (Q1a2a1a1). And, as Q-M3 is mostly found in Yeniseians and Native Americans, the authors suggest that the Xiongnu had connections to speakers of the Yeniseian languages.[159][160] These discoveries from the above papers (Li 2012, Kang et al., 2013) have some positive implications on the not as yet clearly verified theory that the Xiongnu were precursors of the Huns.
- Mongolian noble burials in the Yuan dynasty, Shuzhuanglou Site, northernmost Hebei China, 700YBP: all 3 Q (not analysed subclade, the principal occupant Gaodangwang Korguz (高唐王=趙王 阔里吉思)'s mtDNA=D4m2, two others mtDNA=A)[161]
- (cf) Korguz was a son of a princess of Kublai Khan (元 世祖), and was the king of the Ongud tribe. He died in 1298 and was reburied in Shuzhuanglou in 1311 by his son. (Do not confuse this man with the Uyghur governor, Korguz who died in 1242.) The Ongud tribe (汪古部) was a descendant of the Shatuo tribe (沙陀族) which was a tribe of Göktürks (Western Turkic Khaganate) and was prominent in the Five Dynasties and Ten Kingdoms period of China, building three dynasties. His two queens were all princesses of the Yuan dynasty (Kublai Khan's granddaughters). It was very important for the Yuan dynasty to maintain a marriage alliance with Ongud tribe which had been a principal assistant since Genghis Khan's period. About 16 princesses of the Yuan dynasty married kings of the Ongud tribe.
- Hengbei site (Peng kingdom cemetery of Western Zhou period), Jiang County, Shanxi, 2800-3000YBP: 9 Q1a1-M120, 2 O2a-M95, 1 N, 4 O3a2-P201, 2 O3, 4 O*[156]
See also
[edit]Populations
[edit]Y-DNA Q-M242 subclades
[edit]Y-DNA backbone tree
[edit]References
[edit]- ^ Balanovsky, Oleg; Gurianov, Vladimir; Zaporozhchenko, Valery; Balaganskaya, Olga; Urasin, Vadim; Zhabagin, Maxat; Grugni, Viola; Canada, Rebekah; Al-Zahery, Nadia; Raveane, Alessandro; Wen, Shao-Qing; Yan, Shi; Wang, Xianpin; Zalloua, Pierre; Marafi, Abdullah; Koshel, Sergey; Semino, Ornella; Tyler-Smith, Chris; Balanovska, Elena (February 2017). "Phylogeography of human Y-chromosome haplogroup Q3-L275 from an academic/citizen science collaboration". BMC Evolutionary Biology. 17 (S1): 18. Bibcode:2017BMCEE..17S..18B. doi:10.1186/s12862-016-0870-2. PMC 5333174. PMID 28251872.
- ^ Fagundes, Nelson J. R.; Kanitz, Ricardo; Eckert, Roberta; Valls, Ana C. S.; Bogo, Mauricio R.; Salzano, Francisco M.; Smith, David Glenn; Silva, Wilson A.; Zago, Marco A.; Ribeiro-Dos-Santos, Andrea K.; Santos, Sidney E. B.; Petzl-Erler, Maria Luiza; Bonatto, Sandro L. (2008). "Mitochondrial Population Genomics Supports a Single Pre-Clovis Origin with a Coastal Route for the Peopling of the Americas" (PDF). American Journal of Human Genetics. 82 (3): 583–592. doi:10.1016/j.ajhg.2007.11.013. PMC 2427228. PMID 18313026. Retrieved 2009-11-19.
Since the first studies, it has been found that extant Native American populations exhibit almost exclusively five "mtDNA haplogroups" (A–D and X)6 classified in the autochthonous haplogroups A2, B2, C1, D1, and X2a.7 Haplogroups A–D are found all over the New World and are frequent in Asia, supporting a northeastern Asian origin of these lineages
- ^ a b c d e f g h i Zegura, S. L.; Karafet, TM; Zhivotovsky, LA; Hammer, MF (2004). "High-Resolution SNPs and Microsatellite Haplotypes Point to a Single, Recent Entry of Native American Y Chromosomes into the Americas". Molecular Biology and Evolution. 21 (1): 164–75. doi:10.1093/molbev/msh009. PMID 14595095.
- ^ a b YFull YTree v4.02
- ^ a b Y-DNA Haplogroup Q and its Subclades – 2016
- ^ a b c d Sharma S, Rai E, Bhat AK, Bhanwer AS, Bamezai RN (2007). "A novel subgroup Q5 of human Y-chromosomal haplogroup Q-M242 in India". BMC Evol. Biol. 7 (1): 232. doi:10.1186/1471-2148-7-232. PMC 2258157. PMID 18021436.
- ^ a b c d Karafet, T. M. (2002). "High Levels of Y-Chromosome Differentiation among Native Siberian Populations and the Genetic Signature of a Boreal Hunter-Gatherer Way of Life". Human Biology. 74 (6): 761–789. doi:10.1353/hub.2003.0006. PMID 12617488. S2CID 9443804.
- ^ a b c d Bortolini, Maria-Catira; Salzano, Francisco M.; Thomas, Mark G.; Stuart, Steven; Nasanen, Selja P.K.; Bau, Claiton H.D.; Hutz, Mara H.; Layrisse, Zulay; et al. (September 2003). "Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas". The American Journal of Human Genetics. 73 (3): 524–539. doi:10.1086/377588. PMC 1180678. PMID 12900798.
- ^ Zegura Stephen L., Tatiana M. Karafet, Lev A. Zhivotovsky, Michael F. Hammer. High-Resolution SNPs and Microsatellite Haplotypes Point to a Single, Recent Entry of Native American Y Chromosomes into the Americas, 2004.
- ^ https://www.researchgate.net/publication/310645015_Gene_pool_of_Turkmens_from_Karakalpakstan_in_their_Central_Asian_context_Y-chromosome_polymorphism[full citation needed]
- ^ a b c d e Kharkov, V. N.; Stepanov, V. A.; Medvedeva, O. F.; Spiridonova, M. G.; Voevoda, M. I.; Tadinova, V. N.; Puzyrev, V. P. (2007). "Gene Pool Differences between Northern and Southern Altaians Inferred from the Data on Y-Chromosomal Haplogroups". Genetika. 43 (5): 675–687. doi:10.1134/S1022795407050110. PMID 17633562. S2CID 566825.
- ^ a b Yong-Ke, Zhang; Zheng, Chen; An, FAN; et al. (2009). "Genetic relationships between Tuva population and the neighboring populations in the Altai Region of Xinjiang Uygur Autonomous Region". Yi Chuan = Hereditas. 31 (8): 818–824. doi:10.3724/SP.J.1005.2009.00818. PMID 19689942. S2CID 39635944.
- ^ a b Katharina Olofsson, Jill; et al. (2015). "Peopling of the North Circumpolar Region – Insights from Y Chromosome STR and SNP Typing of Greenlanders". PLOS One. 10 (1): e0116573. Bibcode:2015PLoSO..1016573O. doi:10.1371/journal.pone.0116573. PMC 4312058. PMID 25635810.
- ^ a b Пять генофондов пяти субэтносов сибирских татар
- ^ Estes, Roberta (2020-09-12). "Y DNA Haplogroup P Gets a Brand-New Root – Plus Some Branches". DNAeXplained – Genetic Genealogy. Retrieved 2024-01-21.
- ^ Seielstad, Mark; Yuldasheva, Nadira; Singh, Nadia; Underhill, Peter; Oefner, Peter; Shen, Peidong; Wells, R. Spencer (2003). "A Novel Y-Chromosome Variant Puts an Upper Limit on the Timing of First Entry into the Americas". The American Journal of Human Genetics. 73 (3): 700–705. doi:10.1086/377589. ISSN 0002-9297. PMC 1180698. PMID 12929085.
- ^ Proposed Tree Archived 2011-07-11 at the Wayback Machine
- ^ Krahn, Thomas. "FTDNA Draft Y-DNA Tree (AKA YTree)". Family Tree DNA. Archived from the original on 2015-08-15.
- ^ Karafet, T. M.; Mendez, F. L.; Meilerman, M. B.; Underhill, P. A.; Zegura, S. L.; Hammer, M. F. (2008). "New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree". Genome Research. 18 (5): 830–8. doi:10.1101/gr.7172008. PMC 2336805. PMID 18385274.
- ^ "Y-DNA Haplotree". Family Tree DNA uses the Y-Chromosome Consortium tree and posts it on their website.
- ^ That is because it is a value for the STR DYS435 with a value of 8→9 within haplogroup Q-M242 and the trend is to include only binary markers in phylogenetic trees. However, these are from studies where all current branches of the Q-M242 tree have not been tested. The problematic phylogeny sampling of early studies has been demonstrated by subsequent studies that have found Q-M346, Q-M378, and Q-M25 in South Asia.
- ^ Malhi, RS; Gonzalez-Oliver, A; Schroeder, KB; Kemp, BM; Greenberg, JA; Dobrowski, SZ; Smith, DG; Resendez, A; Karafet, T; Hammer, M; Zegura, S; Brovko, T (2008). "Distribution of Y chromosomes among native North Americans: a study of Athapaskan population history". Am. J. Phys. Anthropol. 137 (4): 412–24. doi:10.1002/ajpa.20883. PMC 2584155. PMID 18618732.
- ^ "Frequency Distribution of Y-DNA Haplogroup Q M3". GeneTree. 2010. Archived from the original on 2009-11-04. Retrieved 2010-01-30.
- ^ a b Rasmussen, Morten; Li, Yingrui; Lindgreen, Stinus; Pedersen, Jakob Skou; Albrechtsen, Anders; Moltke, Ida; Metspalu, Mait; Metspalu, Ene; et al. (February 2010). "Ancient human genome sequence of an extinct Palaeo-Eskimo". Nature. 463 (7282): 757–762. Bibcode:2010Natur.463..757R. doi:10.1038/nature08835. PMC 3951495. PMID 20148029.
- ^ a b Hammer; et al. (Dec 2006). "Population structure of Y chromosome SNP haplogroups in the United States and forensic implications for constructing Y chromosome STR databases". Forensic Sci. Int. 164 (1): 45–55. doi:10.1016/j.forsciint.2005.11.013. PMID 16337103.
- ^ Population Estimates Archived 2014-12-18 at the Wayback Machine
- ^ Vullo, Carlos; et al. (2014). "Association between Y haplogroups and autosomal AIMs reveals intra-population substructure in Bolivian populations". Int J Legal Med. 129 (4): 673–680. doi:10.1007/s00414-014-1025-x. PMID 24878616. S2CID 2906322.
- ^ Söchtig, Jens; et al. (2015). "Genomic insights on the ethno-history of the Maya and the 'Ladinos' from Guatemala". BMC Genomics. 16 (1): 131. doi:10.1186/s12864-015-1339-1. PMC 4422311. PMID 25887241. => Guatemala population consists of about 40% Tribal Natives (Mayans)+60% Native (Spanish Speaking). According to this paper, 89% of Mayan and 25% of Ladinos belong to Y-DNA Q. Thus, 40*0.89+60*0.25=50.6%
- ^ a b c d e f g h i Battaglia; et al. (2013). "The First Peopling of South America: New Evidence from Y-Chromosome Haplogroup Q". PLOS One. 8 (8): e71390. Bibcode:2013PLoSO...871390B. doi:10.1371/journal.pone.0071390. PMC 3749222. PMID 23990949.
- ^ Gaviria, A.; et al. (2013). "Characterization and Haplotype analysis of 11 Y-STR loci in Ecuadorian population". Forensic Sci. Int. Genet. Suppl. 4 (1): e310 – e311. doi:10.1016/j.fsigss.2013.10.158.
- ^ Martínez-Cortés, G; et al. (2012). "Admixture and population structure in Mexican-Mestizos based on paternal lineages". J. Hum. Genet. 57 (9): 568–74. doi:10.1038/jhg.2012.67. PMID 22832385.
- ^ Lovo-Gómez, J; et al. (Sep 2007). "The genetic male legacy from El Salvador". Forensic Sci. Int. 171 (2–3): 198–203. doi:10.1016/j.forsciint.2006.07.005. PMID 16916590.
- ^ Grugni (2015). "Exploring the Y Chromosomal Ancestry of Modern Panamanians". PLOS One. 10 (12): e0144223. Bibcode:2015PLoSO..1044223G. doi:10.1371/journal.pone.0144223. PMC 4670172. PMID 26636572.
- ^ Rojas, Win; et al. (2010). "Genetic Make Up and Structure of Colombian Populations by Means of Uniparental and Biparental DNA Markers". American Journal of Physical Anthropology. 143 (1): 13–20. doi:10.1002/ajpa.21270. PMID 20734436.=> (DANE, 2006) 86% of the whole Colombian population self-reported as of Mixed Ancestry, 3.4% as Native American, 10.5% as African-Columbian. In this paper, 12% (114/954) of MA, 95.7% (135/141) of NA, and 23.8% (5/21) of AC are turned out to be Y-DNA Q. Thus, 86*0.12+3.4*0.957+10.5*0.238=16.1%
- ^ Núñez, Carolina; et al. (2012). "Y chromosome haplogroup diversity in a Mestizo population of Nicaragua". Forensic Sci. Int. Genet. 6 (6): e192 – e195. doi:10.1016/j.fsigen.2012.06.011. PMID 22770600. The author revised his previous paper, genotyping 2 more samples as haplogroup Q by Y-SNP test.
- ^ Corach, Daniel; et al. (2010). "Inferring Continental Ancestry of Argentineans from Autosomal, Y-Chromosomal and Mitochondrial DNA". Annals of Human Genetics. 74 (1): 65–76. doi:10.1111/j.1469-1809.2009.00556.x. hdl:11336/14301. PMID 20059473. S2CID 5908692.
- ^ Ramallo; et al. (Dec 2009). "Comparison of Y-chromosome haplogroup frequencies in eight Provinces of Argentina". Forensic Science International: Genetics Supplement Series. 2 (1): 431–432. doi:10.1016/j.fsigss.2009.08.047.
- ^ Villalta, M.; Rodriguez, A.; González, L.; Arce, V.; Arrieta, G.; Morales, A.; Gusmão, L.; Espinoza, M. (August 2008). "Haplotype data for 12 Y-chromosome STR loci from Costa Rica". Forensic Science International: Genetics Supplement Series. 1 (1): 252–254. doi:10.1016/j.fsigss.2007.10.101.
- ^ Palha, T.; et al. (2012). "Disclosing the Genetic Structure of Brazil through Analysis of Male Lineages with Highly Discriminating Haplotypes". PLOS One. 7 (7): e40007. Bibcode:2012PLoSO...740007P. doi:10.1371/journal.pone.0040007. PMC 3393733. PMID 22808085.=> about 80 out of 2,024 (3.95%) samples in the paper collected from all the regions of Brazil can be classified as Y-DNA Q.
- ^ a b Jeffrey, T.; et al. (Jan 2002). "The Dual Origin and Siberian Affinities of Native American Y Chromosomes". The American Journal of Human Genetics. 70 (1): 192–206. doi:10.1086/338457. PMC 384887. PMID 11731934. The SNPs used in the paper are P-M45, R1a1-M17, Q1a2-M3, and other xP-M45 SNPs. And the author mentions that, among ethnic groups in the paper, R1-M173 is harbored only in some eastern Siberian Udegeys and Koryaks and Native Americans. Also, R2 (distributed in India and its neighbours) cannot be found in far east Siberia. Thus, P-M45 except some samples mentioned above virtually means Q-M242 (xM3). In the paper, 35.3% of Nivkhs and 20.8% of Chukchi people and 18.2% of Siberian Eskimos are shown in P-M45, and 12.5% of Chukchis and 21.2% of Siberian Eskimos are in Q-M3. All of them can be estimated to be in haplogroup Q.
- ^ a b Pakendorf, Brigitte; Novgorodov, Innokentij N.; Osakovskij, Vladimir L.; Danilova, Al’Bina P.; Protod’Jakonov, Artur P.; Stoneking, Mark (2006). "Investigating the effects of prehistoric migrations in Siberia: genetic variation and the origins of Yakuts". Human Genetics. 120 (3): 334–353. doi:10.1007/s00439-006-0213-2. PMID 16845541. S2CID 31651899.
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- ^ The frequencies of Q-M242 shown in both studies (Kim2010, Park2012) are 1.4% (7/506, Kim) and 1.8% (13/706, Park) respectively. But, if recalculated by regional population weights, the adjusted frequencies reach 1.87% (Kim) and 1.91% (Park) respectively, converging to 1.9%.
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- ^ Di Cristofaro, Julie; Pennarun, Erwan; Mazières, Stéphane; Myres, Natalie M.; Lin, Alice A.; Temori, Shah Aga; Metspalu, Mait; Metspalu, Ene; Witzel, Michael; King, Roy J.; Underhill, Peter A.; Villems, Richard; Chiaroni, Jacques (2013-10-18). "Afghan Hindu Kush: Where Eurasian Sub-Continent Gene Flows Converge". PLOS One. 8 (10): e76748. Bibcode:2013PLoSO...876748D. doi:10.1371/journal.pone.0076748. PMC 3799995. PMID 24204668.
- ^ a b c Grugni, Viola; et al. (2012). "Ancient Migratory Events in the Middle East: New Clues from the Y-Chromosome Variation of Modern Iranians". PLOS One. 7 (7): e41252. Bibcode:2012PLoSO...741252G. doi:10.1371/journal.pone.0041252. PMC 3399854. PMID 22815981.
- ^ a b Regueiro, M.; Cadenas, A.M.; Gayden, T.; Underhill, P.A.; Herrera, R.J. (2006). "Iran: Tricontinental Nexus for Y-Chromosome Driven Migration". Human Heredity. 61 (3): 132–143. doi:10.1159/000093774. PMID 16770078. S2CID 7017701.
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- ^ The frequency of Q is 4% (6/150, all Q-M25) in Regueiro 2006, in which it is 9.1% (3/33) in north Iran and 2.6% (3/117) in south Iran. But, since more people live in the northern regions, if recalculated by population weights, the frequency will reach about 6%. It is also 6.2% (35/566) in Bekada 2013 with a large-scale sampling.
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- ^ a b c d e Sengupta, Sanghamitra; Zhivotovsky, Lev A.; King, Roy; Mehdi, S.Q.; Edmonds, Christopher A.; Cheryl-, Cheryl-Emiliane T.; Chow, Emiliane T.; Lin, Alice A.; et al. (2006). "Polarity and Temporality of High-Resolution Y-Chromosome Distributions in India Identify Both Indigenous and Exogenous Expansions and Reveal Minor Genetic Influence of Central Asian Pastoralists". The American Journal of Human Genetics. 78 (2): 202–221. doi:10.1086/499411. PMC 1380230. PMID 16400607.
- ^ Khurana, P; et al. (2014). "Y Chromosome Haplogroup Distribution in Indo-European Speaking Tribes of Gujarat, Western India". PLOS One. 9 (3): e90414. Bibcode:2014PLoSO...990414K. doi:10.1371/journal.pone.0090414. PMC 3948632. PMID 24614885.
- ^ Fornarino, Simona; et al. (2009). "Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation". BMC Evol. Biol. 9 (1): 154. Bibcode:2009BMCEE...9..154F. doi:10.1186/1471-2148-9-154. PMC 2720951. PMID 19573232.
- ^ Nahar Gazi, Nurun; et al. (2013). "Genetic Structure of Tibeto-Burman Populations of Bangladesh: Evaluating the Gene Flow along the Sides of Bay-of-Bengal". PLOS One. 8 (10): e75064. Bibcode:2013PLoSO...875064G. doi:10.1371/journal.pone.0075064. PMC 3794028. PMID 24130682.
- ^ Malyarchuk, B. A.; et al. (2008). "Gene Pool Structure of Russian Populations from the European Part of Russia Inferred from the Data on Y Chromosome Haplogroups Distribution". Russian Journal of Genetics. 44 (2): 187–192. doi:10.1134/S1022795408020105. S2CID 28165493.
- ^ Khar'kov, VN; et al. (Aug 2005). "Frequencies of Y chromosome binary haplogroups in Belarussians". Genetika. 41 (8): 1132–6. doi:10.1007/s11177-005-0182-x. PMID 16161635. S2CID 1357824.
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- ^ Ehler, Edvard; et al. (Jun 2011). "Y-chromosomal diversity of the Valachs from the Czech Republic: model for isolated population in Central Europe". Croat Med J. 52 (3): 358–367. doi:10.3325/cmj.2011.52.358. PMC 3131682. PMID 21674832.
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- ^ Karachanak, Sena; et al. (2013). "Y-Chromosome Diversity in Modern Bulgarians: New Clues about Their Ancestry". PLOS One. 8 (3): e56779. Bibcode:2013PLoSO...856779K. doi:10.1371/journal.pone.0056779. PMC 3590186. PMID 23483890.
- ^ Csányi, B.; et al. (July 2008). "Y-Chromosome Analysis of Ancient Hungarian and Two Modern Hungarian-Speaking Populations from the Carpathian Basin". Annals of Human Genetics. 72 (4): 519–534. doi:10.1111/j.1469-1809.2008.00440.x. PMID 18373723. S2CID 13217908.
- ^ Hungarian Bukovina
- ^ Q-L712 Subclades of haplogroup Q-M25: Q-L712, Q-L715, Q-L713, Q-YP789
- ^ "Family Tree DNA – Genetic Testing for Ancestry, Family History & Genealogy".
- ^ a b c David K. Faux, 2007, The Genetic Link of the Viking – Era Norse to Central Asia: An Assessment of the Y Chromosome DNA, Archaeological, Historical and Linguistic Evidence, http://www.davidkfaux.org/CentralAsiaRootsofScandinavia-Y-DNAEvidence.pdf
- ^ "Family Tree DNA – Genetic Testing for Ancestry, Family History & Genealogy".
- ^ Allison Mann, Vikings, merchants, and pirates at the top of the world : Y-chromosomal signatures of recent and ancient migrations in the Faroe Islands, MA Thesis of University of Louisville, 2012.
- ^ Shetland Islands Haplogroups R1a & Q[usurped]
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