A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402796



Internal ID22460666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18209180..18209631hg38UCSC Ensembl
chr20:18189824..18190275hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945945
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402796
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.50


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