A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934976



Internal ID24049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65259548..65261603hg38UCSC Ensembl
chr3:65245223..65247278hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382056
hg192056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934976
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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