A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931876



Internal ID21981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38500159..38500210hg38UCSC Ensembl
chr3:38541650..38541701hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5395769
Supporting Variants
Samples
Known GenesEXOG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931876
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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