A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108492



Internal ID22017726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36680685..36680685hg38UCSC Ensembl
chr22:37076730..37076730hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641287
Samples
Known GenesCACNG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108492
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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