A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819417



Internal ID15237382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73713455..73714448hg38UCSC Ensembl
Innerchr15:74005796..74006789hg19UCSC Ensembl
Innerchr15:71792849..71793842hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38994
hg19994
hg18994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419147
SamplesAK1
Known GenesCD276
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)nsv819417
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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