A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111653



Internal ID21294919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182560907..182586633hg38UCSC Ensembl
Innerchr4:183482060..183507786hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3825727
hg1925727
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092277
Samplessample243
Known GenesTENM3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111653
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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