A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938689



Internal ID26525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119854365..119855176hg38UCSC Ensembl
chr3:119573212..119574023hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38812
hg19812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449764
Supporting Variants
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938689
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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