A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538468



Internal ID20911785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53633534..53641333hg38UCSC Ensembl
chr20:52250073..52257872hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538468
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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