Variant Details

Variant: esv2663690

Internal ID

9583109

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr10:50102756..50240662	hg38	UCSC Ensembl
Outer	chr10:50102385..50241032	hg38	UCSC Ensembl
Inner	chr10:51862516..52000422	hg19	UCSC Ensembl
Outer	chr10:51862145..52000792	hg19	UCSC Ensembl

Cytoband

10q11.23

Allele length

Assembly	Allele length
hg38	138648
hg19	138648

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv138e199

Supporting Variants

essv6399134, essv5584270, essv6532524, essv6366207, essv6273629, essv6162742, essv5770524, essv5724750, essv5575711, essv6558459, essv5863686, essv5824867, essv5552147, essv6526771, essv5888815, essv6360684, essv5650601, essv6264051, essv5996825, essv5655694, essv6165998, essv5994415, essv5985427, essv5913019, essv5831405, essv5668303, essv6347141, essv5865359, essv6267011, essv6185961, essv6590504, essv5748896, essv5730242, essv6423574, essv6024520, essv5610699, essv5493763, essv6048425, essv6487930, essv5705950, essv5615363, essv6546487, essv6052551, essv6398030, essv5960038, essv5451207, essv5968918, essv6338940, essv6208688, essv5687255, essv5608231

Samples

HG01441, HG01356, HG01462, HG01359, HG01389, HG01374, HG01465, HG01456, HG01461, HG01140, HG01250, HG01350, HG01366, HG01351, HG01488, HG01492, HG01354, HG01365, HG01134, HG01455, HG01495, HG01440, HG01550, HG01124, HG01353, HG01136, HG01360, HG01384, HG01498, HG01149, HG01390, HG01383, HG01497, HG01148, HG01551, HG01253, HG01357, HG01375, HG01494, HG01113, HG01137, HG01489, HG01342, HG01491, HG01254, HG01251, HG01377, HG01378, HG01125, HG01112, HG01437

Known Genes

ASAH2, FAM21A, FAM21B

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2663690

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	51
Observed Complex	0
Frequency	n/a