A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419238



Internal ID15583022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26840460..26841782hg38UCSC Ensembl
Innerchr13:27414597..27415919hg19UCSC Ensembl
Innerchr13:26312597..26313919hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381323
hg191323
hg181323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819258
Supporting Variants
SamplesAK1
Known Genes
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)nssv1419238
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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