A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819181



Internal ID15583882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24861867..24869009hg38UCSC Ensembl
Innerchr15:25107014..25114156hg19UCSC Ensembl
Innerchr15:22658107..22665249hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387143
hg197143
hg187143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419808
SamplesAK1
Known GenesSNRPN
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)nsv819181
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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