A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942152



Internal ID28786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:168899231..168899714hg38UCSC Ensembl
chr3:168617019..168617502hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942152
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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