A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202896



Internal ID20769936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45637501..45647100hg38UCSC Ensembl
chr20:44266140..44275739hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00074


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