A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819585



Internal ID8551275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36661422..36669449hg38UCSC Ensembl
Innerchr14:37130627..37138654hg19UCSC Ensembl
Innerchr14:36200378..36208405hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg388028
hg198028
hg188028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419853
SamplesAK1
Known GenesPAX9
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)nsv819585
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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