A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938192



Internal ID26190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106179574..106188100hg38UCSC Ensembl
chr3:105898421..105906947hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg388527
hg198527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443894
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938192
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001562


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