A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5445673



Internal ID224019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73411597..73411652hg38UCSC Ensembl
chr3:73460748..73460803hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936043
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5445673
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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