A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728608



Internal ID152274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33493300..33504421hg38UCSC Ensembl
chr22:33889286..33900407hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3811122
hg1911122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544834
Supporting Variants
Samples
Known GenesLARGE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728608
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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