A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403322



Internal ID22461192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36921117..36921332hg38UCSC Ensembl
chr22:37317159..37317374hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948363
Supporting Variants
Samples
Known GenesCSF2RB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403322
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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