A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933274



Internal ID22911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46026032..46027403hg38UCSC Ensembl
chr3:46067524..46068895hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381372
hg191372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434820
Supporting Variants
Samples
Known GenesXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933274
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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