A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931635



Internal ID21829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43643181..43643876hg38UCSC Ensembl
chr3:43684673..43685368hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447397
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931635
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006246


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