A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110546



Internal ID21293812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18119747..18125441hg38UCSC Ensembl
Innerchr4:18121370..18127064hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg385695
hg195695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv862n145
Supporting Variantsnssv14092257
Samplessample241
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110546
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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