A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449373



Internal ID227612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73562124..73562981hg38UCSC Ensembl
chr3:73611275..73612132hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936051
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449373
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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