A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459016



Internal ID237035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116068068..116068130hg38UCSC Ensembl
chr6:116389231..116389293hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459016
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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