A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819050



Internal ID15583751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48860981..48862155hg38UCSC Ensembl
Innerchr18:46387352..46388526hg19UCSC Ensembl
Innerchr18:44641350..44642524hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg381175
hg191175
hg181175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419189
SamplesAK1
Known GenesCTIF
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)nsv819050
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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