A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730143



Internal ID153809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34422275..34535511hg38UCSC Ensembl
chr3:34463767..34577003hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38113237
hg19113237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730143
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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