A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097904



Internal ID21287504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33788774..34089444hg38UCSC Ensembl
Innerchr16:33591241..33891911hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38300671
hg19300671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116933
Supporting Variants
Samplessample402
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097904
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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