A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17729111



Internal ID152777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40957337..40957458hg38UCSC Ensembl
chr22:41353341..41353462hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538598
Supporting Variants
Samples
Known GenesRBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17729111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0064


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