A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819467



Internal ID15584168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122092794..122096235hg38UCSC Ensembl
Innerchr9:124855073..124858514hg19UCSC Ensembl
Innerchr9:123894894..123898335hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg383442
hg193442
hg183442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419542
SamplesAK1
Known GenesTTLL11
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)nsv819467
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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