A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065803



Internal ID20632843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:13391874..13394518hg38UCSC Ensembl
chr20:13372521..13375165hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522548
Supporting Variants
Samples
Known GenesTASP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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