A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645708



Internal ID21594013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54306777..54306777hg38UCSC Ensembl
chr16:54340689..54340689hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096533, nssv17085654
SamplesHG03125, HG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645708
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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