A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100259



Internal ID21284396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25027585..25037451hg38UCSC Ensembl
Innerchr18:22607549..22617415hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg389867
hg199867
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116937
Supporting Variants
Samplessample360
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100259
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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