A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931649



Internal ID21839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43861473..43861714hg38UCSC Ensembl
chr3:43902965..43903206hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452455
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931649
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00359


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