A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819173



Internal ID15237138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44926399..44926989hg38UCSC Ensembl
Innerchr14:45395602..45396192hg19UCSC Ensembl
Innerchr14:44465352..44465942hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38591
hg19591
hg18591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419016
SamplesAK1
Known GenesKLHL28
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)nsv819173
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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