A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819597



Internal ID15237562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:57474778..57476427hg38UCSC Ensembl
Innerchr12:57868561..57870210hg19UCSC Ensembl
Innerchr12:56154828..56156477hg18UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg381650
hg191650
hg181650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419299
SamplesAK1
Known GenesARHGAP9
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)nsv819597
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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