A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727809



Internal ID151475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21667960..21668628hg38UCSC Ensembl
chr22:22022249..22022917hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534590
Supporting Variants
Samples
Known GenesPPIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727809
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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