A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1023661



Internal ID15970931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2329296..2365108hg38UCSC Ensembl
Innerchr5:2329410..2365222hg19UCSC Ensembl
Innerchr5:2382410..2418222hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3835813
hg1935813
hg1835813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596910
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)nssv1023661
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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