A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734874



Internal ID158540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73580247..73580302hg38UCSC Ensembl
chr3:73629398..73629453hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139547
Supporting Variants
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734874
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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