A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819078



Internal ID15583779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32057542..32058732hg38UCSC Ensembl
Innerchr15:32349745..32350935hg19UCSC Ensembl
Innerchr15:30137037..30138227hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381191
hg191191
hg181191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419191
SamplesAK1
Known GenesCHRNA7
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)nsv819078
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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