A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940977



Internal ID28021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138888286..138901297hg38UCSC Ensembl
chr3:138607128..138620139hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3813012
hg1913012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940977
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