A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097930



Internal ID21288571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33767563..34089444hg38UCSC Ensembl
Innerchr16:33570030..33891911hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38321882
hg19321882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112414
Supporting Variants
Samplessample419
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097930
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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