A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16963357



Internal ID42898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32207484..32207490hg38UCSC Ensembl
chr5:32207590..32207596hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg383963
hg193963
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561649
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16963357
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005309


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