A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114584



Internal ID21297850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130067688..130074120hg38UCSC Ensembl
Innerchr11:129937583..129944015hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg386433
hg196433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091070
Samplessample149
Known GenesAPLP2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114584
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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