A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930873



Internal ID21335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12441957..12446637hg38UCSC Ensembl
chr3:12483456..12488136hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg384681
hg194681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438572
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930873
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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