A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054667



Internal ID21963901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37044631..37106658hg38UCSC Ensembl
chr20:35673034..35735061hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3862028
hg1962028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623505
Samples
Known GenesMROH8, RBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054667
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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