A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940794



Internal ID27900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148929639..148930093hg38UCSC Ensembl
chr3:148647426..148647880hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445826
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940794
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007337


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