A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051354



Internal ID21960588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35166773..35176647hg38UCSC Ensembl
chr20:33754576..33764450hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg389875
hg199875
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618748
Samples
Known GenesPROCR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051354
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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