A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419303



Internal ID15236357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:117799541..117799766hg38UCSC Ensembl
Innerchr8:118811780..118812005hg19UCSC Ensembl
Innerchr8:118880961..118881186hg18UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38226
hg19226
hg18226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820050
Supporting Variants
SamplesAK1
Known GenesEXT1
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)nssv1419303
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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