A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059949



Internal ID21969182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38948831..38988117hg38UCSC Ensembl
chr22:39344836..39384122hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3839287
hg1939287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638941
Samples
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059949
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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