A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533989



Internal ID20907350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16617901..16619400hg38UCSC Ensembl
chr20:16598546..16600045hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533989
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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