A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562773



Internal ID16350182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95291631..95375253hg38UCSC Ensembl
Innerchr13:95943885..96027507hg19UCSC Ensembl
Innerchr13:94741886..94825508hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3883623
hg1983623
hg1883623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3327n54
Supporting Variantsnssv817540
Samples
Known GenesABCC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562773
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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