A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116736



Internal ID21300002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22314859..22327929hg38UCSC Ensembl
Innerchr10:22603788..22616858hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3813071
hg1913071
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv148n145
Supporting Variantsnssv14088771
Samplessample309
Known GenesBMI1, COMMD3, COMMD3-BMI1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116736
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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