A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118021



Internal ID21301287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152642481..152668368hg38UCSC Ensembl
Innerchr5:152022041..152047928hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3825888
hg1925888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096717
Samplessample17
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118021
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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