A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260082



Internal ID20469300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24336622..24336622hg38UCSC Ensembl
chr16:24347943..24347943hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761207
Supporting Variants
Samples
Known GenesCACNG3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260082
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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