A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520111



Internal ID15447404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51351198..51371169hg38UCSC Ensembl
Innerchr17:49428559..49448530hg19UCSC Ensembl
Innerchr17:46783558..46803529hg18UCSC Ensembl
Innerchr17:46783558..46803529hg17UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3819972
hg1919972
hg1819972
hg1719972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690521, nssv660830
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520111
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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