A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819279



Internal ID15237244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:24812523..24812963hg38UCSC Ensembl
Innerchr12:24965457..24965897hg19UCSC Ensembl
Innerchr12:24856724..24857164hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38441
hg19441
hg18441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418953
SamplesAK1
Known GenesBCAT1
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)nsv819279
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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