A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562959



Internal ID335898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73590333..73590384hg38UCSC Ensembl
chr3:73639484..73639535hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936053
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562959
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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