A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820054



Internal ID15584755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22016530..22146050hg38UCSC Ensembl
Innerchr14:22484770..22614004hg19UCSC Ensembl
Innerchr14:21554610..21683844hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38129521
hg19129235
hg18129235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418781
SamplesAK1
Known Genes
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)nsv820054
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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