A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094975



Internal ID21287686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48482589..48492287hg38UCSC Ensembl
Innerchr4:48484606..48494304hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg389699
hg199699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116213
Supporting Variants
Samplessample404
Known GenesSLC10A4, ZAR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094975
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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