A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728284



Internal ID151950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28169702..28197308hg38UCSC Ensembl
chr22:28565690..28593296hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3827607
hg1927607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553800
Supporting Variants
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728284
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