A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519588



Internal ID15100195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:84841232..85670049hg38UCSC Ensembl
Innerchr4:85762385..86591202hg19UCSC Ensembl
Innerchr4:85981409..86810226hg18UCSC Ensembl
Innerchr4:86119564..86948381hg17UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38828818
hg19828818
hg18828818
hg17828818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694336
Samples
Known GenesARHGAP24, WDFY3, WDFY3-AS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519588
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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