A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519929



Internal ID15100536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60311418..60431257hg38UCSC Ensembl
Innerchr17:58388779..58508618hg19UCSC Ensembl
Innerchr17:55743561..55863400hg18UCSC Ensembl
Innerchr17:55743561..55863400hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38119840
hg19119840
hg18119840
hg17119840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697132
Samples
Known GenesC17orf64, USP32
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519929
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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