A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048563



Internal ID21957796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36679152..36679235hg38UCSC Ensembl
chr22:37075197..37075280hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644263
Samples
Known GenesCACNG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048563
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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