A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931084



Internal ID21472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24038373..24038397hg38UCSC Ensembl
chr3:24079864..24079888hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931084
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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