A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819048



Internal ID15583749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105581638..105856201hg38UCSC Ensembl
Innerchr14:106047975..106322306hg19UCSC Ensembl
Innerchr14:105119020..105393351hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38274564
hg19274332
hg18274332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418798
SamplesAK1
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodOligo aCGH
AnalysisThe array was scanned with Agilent DNA microarray scanner at 2 micron resolution. The resulting image was extracted by Agilent's Feature Extraction software. The log2 ratios were analyzed using NEXUS software. Each aberration call was manually checked to confirm the accuracy of the calls.
PlatformGSE19651
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nsv819048
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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