A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562514



Internal ID16349923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83378798..83456379hg38UCSC Ensembl
Innerchr13:83952933..84030514hg19UCSC Ensembl
Innerchr13:82850934..82928515hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3877582
hg1977582
hg1877582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3286n54
Supporting Variantsnssv816305
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562514
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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