A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048141



Internal ID21957374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43696543..43696987hg38UCSC Ensembl
chr20:42325183..42325627hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626082
Samples
Known GenesMYBL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048141
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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