A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419795



Internal ID15236849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:110135452..110142296hg38UCSC Ensembl
Innerchr12:110573257..110580101hg19UCSC Ensembl
Innerchr12:109057640..109064484hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg386845
hg196845
hg186845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820204
Supporting Variants
SamplesAK1
Known GenesIFT81
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)nssv1419795
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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