A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691624



Internal ID15081590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3390044..3449839hg38UCSC Ensembl
Innerchr17:3293338..3353133hg19UCSC Ensembl
Innerchr17:3240088..3299883hg18UCSC Ensembl
Innerchr17:3240088..3299883hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3859796
hg1959796
hg1859796
hg1759796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521277
Supporting Variants
Samples
Known GenesOR1E1, OR1E2, OR3A3, SPATA22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691624
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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