A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709498



Internal ID133164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58022930..58022947hg38UCSC Ensembl
chr16:58056834..58056851hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709498
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.082111


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