A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115866



Internal ID21299132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22314287..22327757hg38UCSC Ensembl
Innerchr10:22603216..22616686hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3813471
hg1913471
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv148n145
Supporting Variantsnssv14088693
Samplessample263
Known GenesBMI1, COMMD3, COMMD3-BMI1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115866
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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