A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv813689



Internal ID16107645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69188763..69210839hg38UCSC Ensembl
Innerchr13:69762895..69784971hg19UCSC Ensembl
Innerchr13:68660896..68682972hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3822077
hg1922077
hg1822077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562204
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv813689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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