A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109725



Internal ID22018958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36680152..36680152hg38UCSC Ensembl
chr22:37076197..37076197hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639641
Samples
Known GenesCACNG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109725
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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