A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728557



Internal ID152223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32604432..32604473hg38UCSC Ensembl
chr22:33000418..33000459hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535793
Supporting Variants
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728557
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.147101


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