A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937409



Internal ID25664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99432924..99432924hg38UCSC Ensembl
chr3:99151768..99151768hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937409
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.051989


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