A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662845



Internal ID9928950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:37694598..37697304hg38UCSC Ensembl
Outerchr8:37694227..37697674hg38UCSC Ensembl
Innerchr8:37552116..37554822hg19UCSC Ensembl
Outerchr8:37551745..37555192hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383448
hg193448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5866625, essv6013537, essv5506770, essv6472886, essv6100120, essv5411629, essv5820304, essv6404853, essv5944439, essv5933558, essv6049327, essv5968940, essv5491234, essv6131061, essv5524703, essv5640604, essv6504872, essv6480078, essv6147465, essv5892265, essv5602754, essv5961147, essv6310263, essv6557066, essv6161194, essv5639796, essv5451527, essv5557592, essv6118210, essv6235800, essv5599421, essv6344461, essv5471757, essv6422679, essv5942455, essv6050798, essv5488769, essv6540856, essv5598859, essv6023145, essv5664750, essv5597842, essv5554485, essv5491165, essv5489118, essv6189475, essv6306700, essv6029845
SamplesHG00361, HG00318, HG00179, HG00177, HG00327, HG00271, HG00272, HG00330, HG00346, HG00270, HG00185, HG00281, HG00277, HG00335, HG00325, HG00309, HG00182, HG00326, HG00178, HG00323, HG00313, HG00268, HG00266, HG00176, HG00282, HG00328, HG00368, HG00320, HG00344, HG00284, HG00273, HG00373, HG00276, HG00336, HG00285, HG00353, HG00357, HG00319, HG00339, HG00269, HG00312, HG00329, HG00342, HG00174, HG00280, HG00343, HG00274, HG00171
Known GenesZNF703
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662845
Frequency
Sample Size1151
Observed Gain0
Observed Loss48
Observed Complex0
Frequencyn/a


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