A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820034



Internal ID15237999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25209114..25213170hg38UCSC Ensembl
Innerchr8:25066630..25070686hg19UCSC Ensembl
Innerchr8:25122547..25126603hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg384057
hg194057
hg184057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419601
SamplesAK1
Known GenesDOCK5
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)nsv820034
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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