A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116213



Internal ID21299479
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 StatusM
Merged Variantsdgv878n145
Supporting Variantsnssv14094975, nssv14093490
Samplessample404, sample300
Known GenesSLC10A4, ZAR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116213
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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