A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522797



Internal ID15450090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:47006913..47105786hg38UCSC Ensembl
Innerchr17:45084279..45183152hg19UCSC Ensembl
Innerchr17:42439278..42538151hg18UCSC Ensembl
Innerchr17:42439278..42538151hg17UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3898874
hg1998874
hg1898874
hg1798874
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698442
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522797
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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