A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931390



Internal ID21675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30275824..30286903hg38UCSC Ensembl
chr3:30317315..30328394hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3811080
hg1911080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931390
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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