A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114388



Internal ID21297654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22314859..22327757hg38UCSC Ensembl
Innerchr10:22603788..22616686hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3812899
hg1912899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv148n145
Supporting Variantsnssv14089945, nssv14088526
Samplessample184, sample419
Known GenesBMI1, COMMD3, COMMD3-BMI1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114388
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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