A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946990



Internal ID32019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22389308..22392036hg38UCSC Ensembl
chr4:22390931..22393659hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382729
hg192729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438753
Supporting Variants
Samples
Known GenesGPR125
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946990
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