A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672016



Internal ID15061982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46053939..46169798hg38UCSC Ensembl
Innerchr17:44131305..44247164hg19UCSC Ensembl
Innerchr17:41487141..41602941hg18UCSC Ensembl
Innerchr17:41487141..41602941hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38115860
hg19115860
hg18115801
hg17115801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516807
Supporting Variants
Samples
Known GenesKANSL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672016
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer