A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419020



Internal ID15582804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:117146612..117147206hg38UCSC Ensembl
Innerchr8:118158851..118159445hg19UCSC Ensembl
Innerchr8:118228032..118228626hg18UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38595
hg19595
hg18595
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819760
Supporting Variants
SamplesAK1
Known GenesSLC30A8
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)nssv1419020
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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