A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205256



Internal ID20772296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19002354..19013076hg38UCSC Ensembl
chr20:18982998..18993720hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3810723
hg1910723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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