A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819358



Internal ID15237323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22775794..22811167hg38UCSC Ensembl
Innerchr14:23245003..23280376hg19UCSC Ensembl
Innerchr14:22314843..22350216hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3835374
hg1935374
hg1835374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418720
SamplesAK1
Known GenesSLC7A7
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)nsv819358
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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