A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418765



Internal ID15582549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22422811..22510502hg38UCSC Ensembl
Innerchr14:22891802..22979486hg19UCSC Ensembl
Innerchr14:21961642..22049326hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3887692
hg1987685
hg1887685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819847
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)nssv1418765
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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