A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819712



Internal ID15584413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:32916322..32923763hg38UCSC Ensembl
Innerchr14:33385528..33392969hg19UCSC Ensembl
Innerchr14:32455279..32462720hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg387442
hg197442
hg187442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419826
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)nsv819712
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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