A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665327



Internal ID9931432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44733438..44733561hg38UCSC Ensembl
Outerchr21:44733370..44733618hg38UCSC Ensembl
Innerchr21:46153353..46153476hg19UCSC Ensembl
Outerchr21:46153285..46153533hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5762332, essv6259332, essv6543251, essv6532539, essv5750275, essv5597243, essv6291156, essv6438772, essv6259710, essv6116529, essv5642101, essv5542831, essv6360345, essv5623938, essv5944195, essv5809095, essv5766109, essv5694393, essv5411103, essv5590095, essv6567937, essv5907245, essv6316688, essv5932972, essv5451152, essv5618926, essv6138162, essv5910850, essv5539199, essv6569727, essv6019015, essv5701082, essv5478469, essv6375219, essv6000903, essv5482335, essv6137054, essv5731547, essv5721907, essv5406456, essv5835849, essv6522748, essv5697875, essv6559605, essv6508772, essv6038192, essv5853522, essv6172623, essv6421195, essv5551627, essv6368747, essv5996186, essv5619160, essv6190096, essv6572791, essv5447429, essv6465097, essv6209962, essv5438489, essv5955417, essv6272061, essv6406125, essv5500516, essv5901893, essv6446416, essv6225746, essv6405666, essv5938156, essv5870160, essv5796916, essv5852392, essv5491740, essv5794140, essv6358280, essv6306477, essv5581573, essv6216580
SamplesNA19394, HG00542, HG01356, NA19703, HG00671, HG00524, HG01374, HG00318, NA19092, NA18486, HG00699, HG00654, HG00693, HG00663, NA19379, HG01070, NA18597, HG01488, HG00330, NA11992, HG00346, NA19782, NA18611, HG00512, HG00281, HG00277, HG01067, HG01170, NA20340, NA19372, HG00534, NA19317, HG00705, NA19189, HG00530, HG01353, HG00653, NA20760, HG00436, NA19982, HG00583, HG00500, HG00263, HG00708, HG00692, HG01047, HG00690, HG00331, HG00684, NA18532, HG00463, NA19318, NA18570, HG01107, NA19834, NA19747, HG00580, HG00136, HG00278, HG00607, NA19360, NA19818, HG00614, HG00329, HG00656, NA19093, NA20289, HG00310, NA18873, NA20807, HG00698, HG00343, HG00377, HG01377, HG01378, HG01125, NA18522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665327
Frequency
Sample Size1151
Observed Gain0
Observed Loss77
Observed Complex0
Frequencyn/a


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