A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692801



Internal ID15429453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3310434..3317250hg38UCSC Ensembl
Innerchr17:3213728..3220544hg19UCSC Ensembl
Innerchr17:3160478..3167294hg18UCSC Ensembl
Innerchr17:3160478..3167294hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg386817
hg196817
hg186817
hg176817
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520474
Supporting Variants
Samples
Known GenesOR3A4P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692801
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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