A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152992



Internal ID15875680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:4647914..4661399hg38UCSC Ensembl
Innerchr5:4648027..4661512hg19UCSC Ensembl
Innerchr5:4701027..4714512hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3813486
hg1913486
hg1813486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596931
Supporting Variants
SamplesHGDP00721
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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