A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728758



Internal ID152424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36200337..36233797hg38UCSC Ensembl
chr22:36596383..36629843hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3833461
hg1933461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540224
Supporting Variants
Samples
Known GenesAPOL2, APOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728758
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000157


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