A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945931



Internal ID31296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192963574..192969680hg38UCSC Ensembl
chr3:192681363..192687469hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg386107
hg196107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945931
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002975


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