Variant Details

Variant: esv2670790

Internal ID

9936895

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr8:21352535..21352802	hg38	UCSC Ensembl
	chr8:21210046..21210313	hg19	UCSC Ensembl

Cytoband

8p21.3

Allele length

Assembly	Allele length
hg38	268
hg19	268

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5803687, essv5441542, essv6175269, essv5442740, essv5948702, essv5800612, essv6387590, essv5726534, essv6248696, essv6069650, essv6555310, essv6230363, essv6477558, essv6362010, essv6192086, essv5540056, essv5704470, essv5521630, essv5535298, essv6360025, essv6483322, essv5637985, essv5543027, essv5613078, essv5590642, essv5853081, essv6564357, essv5884641, essv5786921, essv6172697, essv5630554, essv5688821, essv5504120, essv6521708, essv6532252, essv6049084, essv6470069, essv6320916, essv5857295, essv5859485, essv5427351, essv6434333, essv6524051, essv5926882, essv5989236, essv6071472, essv6338168, essv6488495, essv5721787, essv5520621, essv6196781, essv5491552, essv6253074, essv6052913, essv5620963, essv6395899

Samples

NA18502, HG01462, NA19204, NA19350, NA18486, NA19190, HG01051, NA18510, NA07346, NA19374, NA19373, NA19171, NA19119, NA11992, NA07347, NA18582, NA19384, HG01110, NA18949, NA19383, NA19917, HG01072, NA19238, NA11994, NA19239, NA18975, NA11831, NA18951, NA19403, NA19347, NA19152, NA18516, NA18910, NA18871, NA18572, NA18948, HG01197, NA19099, NA12144, NA18523, NA19160, NA18945, NA18974, NA18608, NA18953, NA19440, NA19390, NA19834, NA19240, NA19311, NA19818, NA19376, NA18609, NA20322, NA19346, NA19676

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2670790

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	56
Observed Complex	0
Frequency	n/a