A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671146



Internal ID21619451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60021897..60021897hg38UCSC Ensembl
chr20:58596952..58596952hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117515
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671146
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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