A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820242



Internal ID15584943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102728597..102729709hg38UCSC Ensembl
Innerchr10:104488354..104489466hg19UCSC Ensembl
Innerchr10:104478344..104479456hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381113
hg191113
hg181113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419175
SamplesAK1
Known GenesSFXN2
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)nsv820242
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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