A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761207



Internal ID20537067
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 StatusM
Merged Variants
Supporting Variantsnssv16260082
Samples
Known GenesCACNG3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761207
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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