A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148667



Internal ID15872884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88219504..88328018hg38UCSC Ensembl
Innerchr13:88871759..88980273hg19UCSC Ensembl
Innerchr13:87669760..87778274hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38108515
hg19108515
hg18108515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562633
Supporting Variants
SamplesHGDP00064
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148667
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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