A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118277



Internal ID21301543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48482589..48492587hg38UCSC Ensembl
Innerchr4:48484606..48494604hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg389999
hg199999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv878n145
Supporting Variantsnssv14094820
Samplessample378
Known GenesSLC10A4, ZAR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118277
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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