A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048902



Internal ID21958136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23274639..23276124hg38UCSC Ensembl
chr22:23616826..23618311hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg381486
hg191486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639346
Samples
Known GenesBCR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048902
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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