A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697356



Internal ID15087322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3553441..3559573hg38UCSC Ensembl
Innerchr17:3456735..3462867hg19UCSC Ensembl
Innerchr17:3403485..3409617hg18UCSC Ensembl
Innerchr17:3403485..3409617hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg386133
hg196133
hg186133
hg176133
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516676
Supporting Variants
Samples
Known GenesTRPV3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697356
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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