A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651298



Internal ID21599603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24316244..24316244hg38UCSC Ensembl
chr16:24327565..24327565hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091029
SamplesHG00731
Known GenesCACNG3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651298
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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