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Haplogroup Q-P89.1

Human Y-chromosome DNA haplogroup

Human Y-chromosome DNA haplogroup

FieldValue
nameQ-P89.1
origin-dateInsufficient data
origin-placeAsia or Beringia
ancestorQ-MEH2
mutationsP89.1

| origin-date = Insufficient data | origin-place = Asia or Beringia Haplogroup Q-P89.1 is a subclade of Y-DNA Haplogroup Q-MEH2. Haplogroup Q-P89.1 is defined by the presence of the P89.1 Single Nucleotide Polymorphism (SNP). In 2010, Q-P89.1 was reclassified as "private" and removed from the haplotree.

Distribution

Q-P89.1 has descendants in the Northwest Territory of modern Canada. It was in pre-Columbian American populations that it was discovered.

The Americas

Q-P89.1 is present in pre-Columbian populations in the Canadian Northwest.

PopulationPaperNPercentageSNP Tested
Gwich’in
Tłįchǫ
Inuvialuit
Inupiat

Asia

Because samples from Asia have only sporadically been tested for this lineage, its frequency there is uncertain.

Associated SNPs

Q-P89.1 is currently defined by only the P89.1 SNP.

References

References

  1. (2012). "Y-chromosome analysis reveals genetic divergence and new founding native lineages in Athapaskan- and Eskimoan-speaking populations". Proceedings of the National Academy of Sciences.
  2. (March 23, 2021). "Y-DNA Haplogroup Q and its Subclades - 2010". ISOGG.
  3. (2008). "New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree". Genome Research.
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