A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819768



Internal ID15237733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69480126..69512183hg38UCSC Ensembl
Innerchr9:72095042..72127099hg19UCSC Ensembl
Innerchr9:71284862..71316919hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3832058
hg1932058
hg1832058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418719
SamplesAK1
Known GenesAPBA1
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)nsv819768
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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