A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098631



Internal ID21285722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:48615045..48615865hg38UCSC Ensembl
Innerchr17:46692407..46693227hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115515
Supporting Variants
Samplessample379
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098631
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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