A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055257



Internal ID21964490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19243758..19247621hg38UCSC Ensembl
chr22:19231281..19235144hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg383864
hg193864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648307
Samples
Known GenesCLTCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055257
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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