A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728341



Internal ID152007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29061492..29065044hg38UCSC Ensembl
chr22:29457480..29461032hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg383553
hg193553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535803
Supporting Variants
Samples
Known GenesC22orf31
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728341
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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