Variant Details

Variant: esv2657877

Internal ID

9577296

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr8:32157300..32159406	hg38	UCSC Ensembl
Outer	chr8:32156829..32159776	hg38	UCSC Ensembl
Inner	chr8:32014816..32016922	hg19	UCSC Ensembl
Outer	chr8:32014345..32017292	hg19	UCSC Ensembl

Cytoband

8p12

Allele length

Assembly	Allele length
hg38	2948
hg19	2948

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6005591, essv6427220, essv6315504, essv6126587, essv5479433, essv6507289, essv5951251, essv5586885, essv5818927, essv6348639, essv6219443, essv6449820, essv6249600, essv5718912, essv5945356, essv5903128, essv5523852, essv6013829, essv5554493, essv6138975, essv6502372, essv6531773, essv6544968, essv6286613, essv6470390, essv5883229, essv6446430, essv6317260, essv5794661, essv5678869, essv5438110, essv6163211, essv5769989, essv5701821, essv6065827, essv5817837, essv6152220, essv6377670, essv5665053, essv6104008, essv5543255, essv5983827, essv5669844, essv5857562, essv6366782, essv6399003, essv5476298, essv5853895, essv5769829, essv5404900, essv5963108, essv6536811, essv6486511, essv5438622, essv6077450, essv5706923, essv6313354, essv5486995, essv6404805, essv6007340, essv5995276, essv5687054, essv6332754, essv6195729, essv5562834, essv5544633, essv6588127, essv5759639, essv5756812, essv6326961, essv6063404, essv6480217, essv6342708, essv5653200, essv6079523, essv6542704, essv5773239, essv6169566

Samples

HG01060, HG01173, HG01052, HG01079, HG01188, HG01066, HG00315, HG00640, HG00318, HG00737, HG00179, HG01051, HG00337, HG00327, HG00271, HG00641, HG01070, HG00173, HG00330, HG00736, HG00346, HG01083, HG00270, HG00334, HG00281, HG00277, HG01080, HG01067, HG00335, HG01170, HG00325, HG01072, HG00309, HG00338, HG01048, HG00326, HG00323, HG01183, HG00731, HG00266, HG00176, HG01171, HG00328, HG00732, HG00320, HG00275, HG01047, HG01102, HG00324, HG00284, HG01073, HG01197, HG00331, HG01101, HG00321, HG00276, HG01107, HG01075, HG00336, HG00285, HG00353, HG00375, HG00734, HG00638, HG00278, HG01174, HG00319, HG01108, HG00339, HG01055, HG00280, HG00343, HG00372, HG00274, HG01082, HG00345, HG01097, HG01061

Known Genes

NRG1

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2657877

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	78
Observed Complex	0
Frequency	n/a