A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098267



Internal ID21285820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2648574..2687214hg38UCSC Ensembl
Innerchr16:2698575..2737215hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3838641
hg1938641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116141
Supporting Variants
Samplessample38
Known GenesERVK13-1, KCTD5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098267
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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