A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819223



Internal ID8550913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27656300..27656593hg38UCSC Ensembl
Innerchr11:27677847..27678140hg19UCSC Ensembl
Innerchr11:27634423..27634716hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38294
hg19294
hg18294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419792
SamplesAK1
Known GenesBDNF, BDNF-AS
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)nsv819223
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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