A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407771



Internal ID22465641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35220286..35221338hg38UCSC Ensembl
chr20:33808089..33809141hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381053
hg191053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407771
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.016


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