A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931666



Internal ID21851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44031354..44031393hg38UCSC Ensembl
chr3:44072846..44072885hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931666
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002498


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