A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418870



Internal ID15582654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131234195..131234553hg38UCSC Ensembl
Innerchr9:134109582..134109940hg19UCSC Ensembl
Innerchr9:133099403..133099761hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38359
hg19359
hg18359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819444
Supporting Variants
SamplesAK1
Known GenesNUP214
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)nssv1418870
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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