A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930426



Internal ID21026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30696983..30697626hg38UCSC Ensembl
chr3:30738475..30739118hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444613
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930426
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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