A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523232



Internal ID15450525
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698955
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523232
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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