A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644668



Internal ID21836715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23234669..23235625hg38UCSC Ensembl
chr22:23576856..23577812hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054978
Supporting Variants
Samples
Known GenesBCR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644668
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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