A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931658



Internal ID21845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43937848..43943421hg38UCSC Ensembl
chr3:43979340..43984913hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg385574
hg195574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931658
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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