A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819298



Internal ID15583999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128649651..128654141hg38UCSC Ensembl
Innerchr9:131411930..131416420hg19UCSC Ensembl
Innerchr9:130451751..130456241hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384491
hg194491
hg184491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419640
SamplesAK1
Known GenesWDR34
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)nsv819298
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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