A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419049



Internal ID15582833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67202015..67202686hg38UCSC Ensembl
Innerchr15:67494353..67495024hg19UCSC Ensembl
Innerchr15:65281407..65282078hg18UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg38672
hg19672
hg18672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819309
Supporting Variants
SamplesAK1
Known GenesAAGAB
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)nssv1419049
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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