A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520881



Internal ID15448174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72218857..72250567hg38UCSC Ensembl
Innerchr17:70214998..70246708hg19UCSC Ensembl
Innerchr17:67726593..67758303hg18UCSC Ensembl
Innerchr17:67726593..67758303hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3831711
hg1931711
hg1831711
hg1731711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697667
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520881
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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