A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819115



Internal ID15583816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8768403..8769706hg38UCSC Ensembl
Innerchr3:8810089..8811392hg19UCSC Ensembl
Innerchr3:8785089..8786392hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381304
hg191304
hg181304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419230
SamplesAK1
Known GenesOXTR
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)nsv819115
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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