A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695051



Internal ID15085017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10282655..10291344hg38UCSC Ensembl
Innerchr17:10185972..10194661hg19UCSC Ensembl
Innerchr17:10126697..10135386hg18UCSC Ensembl
Innerchr17:10126697..10135386hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg388690
hg198690
hg188690
hg178690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520771
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695051
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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