A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066582



Internal ID20633622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16580474..16584761hg38UCSC Ensembl
chr20:16561119..16565406hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg384288
hg194288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00025


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