A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528490



Internal ID20901851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20191704..20360248hg38UCSC Ensembl
chr20:20172348..20340892hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38168545
hg19168545
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205265
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528490
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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