A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523920



Internal ID15451213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5825840..5991845hg38UCSC Ensembl
Innerchr5:5825953..5991958hg19UCSC Ensembl
Innerchr5:5878953..6044958hg18UCSC Ensembl
Innerchr5:5878953..6044958hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38166006
hg19166006
hg18166006
hg17166006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699763
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523920
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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