A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728219



Internal ID151885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26791023..26791023hg38UCSC Ensembl
chr22:27186986..27186986hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538490
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728219
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