A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv809839



Internal ID16103795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41849570..42005392hg38UCSC Ensembl
Innerchr13:42423706..42579528hg19UCSC Ensembl
Innerchr13:41321706..41477528hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38155823
hg19155823
hg18155823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561541
Supporting Variants
Samples
Known GenesVWA8, VWA8-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv809839
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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