A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2656665

Internal ID9576084
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1409616..1410035hg38UCSC Ensembl
Outerchr10:1409579..1410085hg38UCSC Ensembl
Innerchr10:1451811..1452230hg19UCSC Ensembl
Outerchr10:1451774..1452280hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5926796, essv6188321, essv6383628, essv5577971, essv5853011, essv6065876, essv5605235, essv5487850, essv5648173, essv5714188, essv5805421, essv5868122, essv6196248, essv5407015, essv5698705, essv6560686, essv6369527, essv5844313, essv6194806, essv5794883, essv6133829, essv6547587, essv6137332, essv5507441, essv5450909, essv6477493, essv5995989, essv5805428, essv5806617, essv6001467, essv6160741, essv5991694, essv5675244, essv6592855, essv6040855, essv5794265, essv5567888, essv5651296, essv5891534, essv5932988, essv5551551, essv5922491, essv6545387, essv5499663, essv6258083, essv6318360, essv6149696, essv6203947, essv5850758, essv6307999, essv6028264, essv6210766, essv5701726, essv6175062, essv5662279, essv5782541, essv6416174, essv5481517, essv5767828, essv5456269, essv5441227, essv5844582
SamplesHG01515, HG00607, HG01353, NA18530, NA12286, HG01075, HG00127, HG00369, HG01083, HG00731, NA19093, HG01098, HG01492, HG00375, HG01491, NA19685, HG00187, HG00737, NA18557, NA20755, NA18596, HG00269, HG00244, NA19077, HG00154, HG01375, HG00583, HG01378, NA19088, HG00533, NA20765, NA19773, HG00284, HG00114, HG00159, NA19657, HG01073, HG00239, HG01170, HG00249, NA18564, NA18942, HG00329, HG00534, NA19707, HG00236, NA18619, NA18987, NA18999, NA20581, HG01137, NA18567, NA18565, NA19747, NA20287, HG01390, HG00530, HG01251, HG01125, NA19756, NA19750, HG00361
Known GenesADARB2
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2656665
Sample Size1151
Observed Gain0
Observed Loss62
Observed Complex0

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