A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402110



Internal ID22459980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16241068..16241732hg38UCSC Ensembl
chr20:16221713..16222377hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931965
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402110
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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