A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv811794



Internal ID16105750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55030298..55050589hg38UCSC Ensembl
Innerchr13:55604433..55624724hg19UCSC Ensembl
Innerchr13:54502434..54522725hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3820292
hg1920292
hg1820292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561705
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)nssv811794
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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