A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139547



Internal ID338734
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 StatusM
Merged Variants
Supporting Variantsnssv17734874
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139547
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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