A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118285



Internal ID21301551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124214574..124225184hg38UCSC Ensembl
Innerchr11:124085281..124095889hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3810611
hg1910609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv228n145
Supporting Variantsnssv14093148
Samplessample322
Known GenesOR8G2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118285
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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