A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709685



Internal ID133351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83950364..83950980hg38UCSC Ensembl
chr16:83983969..83984585hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709685
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.549813


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