A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110966



Internal ID21294232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106019404..106033329hg38UCSC Ensembl
Innerchr4:106940561..106954486hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3813926
hg1913926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090543
Samplessample160
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110966
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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