A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662273



Internal ID15052239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3553441..3601921hg38UCSC Ensembl
Innerchr17:3456735..3505215hg19UCSC Ensembl
Innerchr17:3403485..3451964hg18UCSC Ensembl
Innerchr17:3403485..3451964hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3848481
hg1948481
hg1848480
hg1748480
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)nssv662273
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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