Genetic Homeland DNA Marker Index for CTS9996.1 on Y chromosome

DNA Marker Index information for Chromosome: Y Marker: CTS9996.1
Names and Aliases for this DNA Marker: CTS9996.1, CTS9996, rs774793025.
Chromosome Position in hg38 Human Genome assembly¹: 17085017.
Chromosome Position in hg19 assembly²: 19196897 .
Ancestral marker allele value: G.
Derived, alternative, or mutated marker allele value: A.

DNA Marker Index data for Marker: CTS9996.1 on Chromosome: Y
Marker Name(s) (separated with a single space)	Notes	Identification	Ancestral⁷	Derived⁸	Chromosome	Position (hg38)¹	Position (hg19)²
O-CTS9996 CTS9996.1 CTS9996 rs774793025	Found in haplogroup O1b under F3016 and Page59 on FTDNA, ISOGG, and 23mofang trees. Believed coincident with Z24289 on YFull tree. Believed ancestor to PF4341 based on markers not shared. See also CTS9996.2 in haplogroup O2a. DNA lineage CTS9996.1 is estimated to have originated in about the year 15,500 bce based on its position in the phylogenetic tree. Phylogenetic Parent: Page59 View Ancestry Phylogenetic Children: CTS298.1 MF14344 NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 17706291	Chris Tyler-Smith 2011	G	A	Y	17085017	19196897

Links for more information

DNA Pedigree by SNP Markers
Marker & Branch Count by Haplogroup
ISOGG Tree page which (at bottom of page) includes a list of the SNP marker prefixes and the entity which published those markers.
DNA Mapping Projects
ISOGG YBrowse tool
ISOGG Y-DNA Hapogroup Tree
ISOGG Index of FTDNA FT-- series markers from Big Y-700 testing.
YFull Y Tree
FTDNA Public Y-DNA Haplotree
23mofang Y Tree Y 遗传标记树
YTree.Net mutations by Alex Williamson. Focused on R-P312 and subbranches.
Irish Type III Website with authoritative list of DC marker series by Dennis Wright
YFull MtDNA Tree
SNPedia.com database for any chromosome
Ancient DNA on Indo-European.eu by Carlos Quiles (and formerly Jean Manco)
Legacy Y-STR Marker Conversion Notes
Geographic Map Site Index

DNA Marker Index data for Marker: CTS9996.1 on Chromosome: Y

Links for more information

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