A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092277



Internal ID21276885
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 StatusS
Merged Variantsnsv3111653
Supporting Variants
Samplessample243
Known GenesTENM3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092277
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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