A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616086



Internal ID21564391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36879577..36879577hg38UCSC Ensembl
chr3:36921068..36921068hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136208
SamplesNA19238
Known GenesTRANK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616086
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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