A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653866



Internal ID21602171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24336650..24336650hg38UCSC Ensembl
chr16:24347971..24347971hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083687
SamplesNA24385
Known GenesCACNG3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653866
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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