A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058448



Internal ID21967681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21209594..21209800hg38UCSC Ensembl
chr20:21190232..21190438hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632842
Samples
Known GenesPLK1S1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058448
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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