A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707485



Internal ID131151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67198847..67198898hg38UCSC Ensembl
chr16:67232750..67232801hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416053
Supporting Variants
Samples
Known GenesE2F4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707485
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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