A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116882



Internal ID21300148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58933968..58940838hg38UCSC Ensembl
Innerchr16:58967872..58974742hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386871
hg196871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098371, nssv14098221, nssv14096411, nssv14099282, nssv14099228, nssv14098305, nssv14099275
Samplessample53, sample87, sample223, sample10, sample227, sample197, sample273
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116882
Frequency
Sample Size467
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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