A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117496



Internal ID21300762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31646479..31663948hg38UCSC Ensembl
Innerchr17:29973498..29990967hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3817470
hg1917470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098129
Samplessample88
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117496
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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