A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642889



Internal ID21834936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42828192..42828333hg38UCSC Ensembl
chr22:43224198..43224339hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042239
Supporting Variants
Samples
Known GenesARFGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642889
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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