A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016583



Internal ID21925926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79386106..79391264hg38UCSC Ensembl
chr8:80298341..80303499hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg385159
hg195159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016583
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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