A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656665



Internal ID9576084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1409616..1410035hg38UCSC Ensembl
Outerchr10:1409579..1410085hg38UCSC Ensembl
Innerchr10:1451811..1452230hg19UCSC Ensembl
Outerchr10:1451774..1452280hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38507
hg19507
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
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656665
Frequency
Sample Size1151
Observed Gain0
Observed Loss62
Observed Complex0
Frequencyn/a


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