A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819780



Internal ID15237745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1511545..1513263hg38UCSC Ensembl
Innerchr10:1553740..1555458hg19UCSC Ensembl
Innerchr10:1543740..1545458hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381719
hg191719
hg181719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419311
SamplesAK1
Known GenesADARB2
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)nsv819780
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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