A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641287



Internal ID21833334
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 StatusS
Merged Variantsnsv6108492
Supporting Variants
Samples
Known GenesCACNG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641287
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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