A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114876



Internal ID21298142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18119397..18125441hg38UCSC Ensembl
Innerchr4:18121020..18127064hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg386045
hg196045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv862n145
Supporting Variantsnssv14090610, nssv14107358, nssv14092371
Samplessample266, sample171, sample44
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114876
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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