A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819112



Internal ID15237077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133058467..133082220hg38UCSC Ensembl
Innerchr9:135933854..135957607hg19UCSC Ensembl
Innerchr9:134923675..134947428hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3823754
hg1923754
hg1823754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418694
SamplesAK1
Known GenesCEL, GTF3C5
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)nsv819112
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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