A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2657877

Internal ID9577296
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:32157300..32159406hg38UCSC Ensembl
Outerchr8:32156829..32159776hg38UCSC Ensembl
Innerchr8:32014816..32016922hg19UCSC Ensembl
Outerchr8:32014345..32017292hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6486511, essv6152220, essv6399003, essv6079523, essv6507289, essv6317260, essv5963108, essv5479433, essv6195729, essv6446430, essv6313354, essv6326961, essv5857562, essv5701821, essv5718912, essv5678869, essv6063404, essv6404805, essv5794661, essv6315504, essv5759639, essv5818927, essv6249600, essv6480217, essv5476298, essv6531773, essv5883229, essv6536811, essv6126587, essv6348639, essv5554493, essv5983827, essv5544633, essv6366782, essv5665053, essv5523852, essv5769989, essv5945356, essv6502372, essv5438622, essv6104008, essv6013829, essv6005591, essv6544968, essv5853895, essv6065827, essv6163211, essv5486995, essv6138975, essv5669844, essv5773239, essv5586885, essv6542704, essv6588127, essv6332754, essv6286613, essv6449820, essv5817837, essv5438110, essv6342708, essv5404900, essv5653200, essv6470390, essv5903128, essv6007340, essv6077450, essv5951251, essv6169566, essv6377670, essv5706923, essv5543255, essv5756812, essv6219443, essv5562834, essv6427220, essv5769829, essv5687054, essv5995276
SamplesHG00323, HG00309, HG00734, HG00318, HG01072, HG01052, HG01075, HG00328, HG01055, HG01173, HG01083, HG00274, HG00731, HG00736, HG01079, HG01197, HG01051, HG01082, HG00375, HG01174, HG00173, HG00326, HG00270, HG01188, HG00334, HG00280, HG00335, HG01101, HG00331, HG00319, HG00737, HG01171, HG00353, HG00266, HG01107, HG00321, HG00339, HG00346, HG00179, HG00337, HG00638, HG01048, HG01061, HG00372, HG01183, HG01047, HG00315, HG00330, HG00338, HG00276, HG00284, HG00343, HG01097, HG00640, HG01066, HG00732, HG00325, HG00176, HG01073, HG01170, HG00277, HG01080, HG01070, HG01060, HG00281, HG00285, HG01108, HG00320, HG00275, HG00324, HG00641, HG01102, HG00336, HG00345, HG00271, HG00278, HG01067, HG00327
Known GenesNRG1
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2657877
Sample Size1151
Observed Gain0
Observed Loss78
Observed Complex0

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