A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698955



Internal ID15435607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:123824404..123857251hg38UCSC Ensembl
Innerchr5:123160098..123192945hg19UCSC Ensembl
Innerchr5:123187997..123220844hg18UCSC Ensembl
Innerchr5:123187997..123220844hg17UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3832848
hg1932848
hg1832848
hg1732848
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523232
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698955
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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