A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933021



Internal ID22737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58440279..58443061hg38UCSC Ensembl
chr3:58426006..58428788hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg382783
hg192783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445735
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933021
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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