A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602761



Internal ID16390170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32644878..32658342hg38UCSC Ensembl
Innerchr6:32612655..32626119hg19UCSC Ensembl
Innerchr6:32720633..32734097hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3813465
hg1913465
hg1813465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10595n54
Supporting Variantsnssv1056785, nssv1056783, nssv1056786, nssv1056791, nssv1056789, nssv1056787, nssv1056788, nssv1056790, nssv1056784
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602761
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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