A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820290



Internal ID15584991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121181543..121182897hg38UCSC Ensembl
Innerchr9:123943821..123945175hg19UCSC Ensembl
Innerchr9:122983642..122984996hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381355
hg191355
hg181355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419243
SamplesAK1
Known GenesRAB14
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)nsv820290
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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