A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419391



Internal ID15583175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:53129306..53131443hg38UCSC Ensembl
Innerchr13:53703441..53705578hg19UCSC Ensembl
Innerchr13:52601442..52603579hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg382138
hg192138
hg182138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819784
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)nssv1419391
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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