A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066888



Internal ID20633928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24130282..24130682hg38UCSC Ensembl
chr20:24110918..24111318hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00113


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