A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931487



Internal ID21736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34186728..34196315hg38UCSC Ensembl
chr3:34228220..34237807hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg389588
hg199588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931487
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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