A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528514



Internal ID15455807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46902339..46905815hg38UCSC Ensembl
Innerchr17:44979705..44983181hg19UCSC Ensembl
Innerchr17:42334704..42338180hg18UCSC Ensembl
Innerchr17:42334704..42338180hg17UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg383477
hg193477
hg183477
hg173477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705121
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528514
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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