A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670098



Internal ID15060064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3553441..3597216hg38UCSC Ensembl
Innerchr17:3456735..3500510hg19UCSC Ensembl
Innerchr17:3403485..3447259hg18UCSC Ensembl
Innerchr17:3403485..3447259hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3843776
hg1943776
hg1843775
hg1743775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516676
Supporting Variants
Samples
Known GenesTRPV1, TRPV3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670098
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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