A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641750



Internal ID21833797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21668993..21669132hg38UCSC Ensembl
chr22:22023282..22023421hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041046
Supporting Variants
Samples
Known GenesPPIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641750
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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