A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940220



Internal ID27524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161605508..161605559hg38UCSC Ensembl
chr3:161323296..161323347hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5408322
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940220
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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