A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020580



Internal ID21929923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65321683..65323138hg38UCSC Ensembl
chr16:65355586..65357041hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381456
hg191456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636254
Samples
Known GenesLINC00922
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020580
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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