A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068120



Internal ID20635160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45234864..45236224hg38UCSC Ensembl
chr20:43863505..43864865hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381361
hg191361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00089


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