A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933313



Internal ID22936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46554265..46554317hg38UCSC Ensembl
chr3:46595755..46595807hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441043
Supporting Variants
Samples
Known GenesLRRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933313
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.406721


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