A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993722



Internal ID21903065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49322352..49325193hg38UCSC Ensembl
chr3:49359785..49362626hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382842
hg192842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542204
Samples
Known GenesUSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993722
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer