A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651255



Internal ID21599560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59615880..59615880hg38UCSC Ensembl
chr16:59649784..59649784hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080866
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651255
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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