A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096526



Internal ID21282779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65142617..65143403hg38UCSC Ensembl
Innerchr16:65176520..65177306hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116668
Supporting Variants
Samplessample331
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096526
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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