A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670190



Internal ID15406842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51417214..51475315hg38UCSC Ensembl
Innerchr17:49494575..49552676hg19UCSC Ensembl
Innerchr17:46849574..46907675hg18UCSC Ensembl
Innerchr17:46849574..46907675hg17UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3858102
hg1958102
hg1858102
hg1758102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516691
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670190
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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