A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667677



Internal ID21615982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35220286..35220286hg38UCSC Ensembl
chr20:33808089..33808089hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381053
hg191053
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116856
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667677
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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