A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17539445



Internal ID21863800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65305590..65306512hg38UCSC Ensembl
chr3:65291265..65292187hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38923
hg19923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993893
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17539445
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