A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418701



Internal ID15582485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129421928..129447270hg38UCSC Ensembl
Innerchr9:132184207..132209549hg19UCSC Ensembl
Innerchr9:131224028..131249370hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3825343
hg1925343
hg1825343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819778
Supporting Variants
SamplesAK1
Known Genes
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)nssv1418701
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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