A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820177



Internal ID15238142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:52878549..52879133hg38UCSC Ensembl
Innerchr14:53345267..53345851hg19UCSC Ensembl
Innerchr14:52415017..52415601hg18UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38585
hg19585
hg18585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419012
SamplesAK1
Known GenesFERMT2
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)nsv820177
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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