A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940387



Internal ID27640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143185004..143185377hg38UCSC Ensembl
chr3:142903846..142904219hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434482
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940387
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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