A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026227



Internal ID21935570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58205111..58214476hg38UCSC Ensembl
chr13:58779245..58788610hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg389366
hg199366
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026227
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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