A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819187



Internal ID15237152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34379376..34575577hg38UCSC Ensembl
Innerchr15:34671577..34867778hg19UCSC Ensembl
Innerchr15:32458869..32655070hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38196202
hg19196202
hg18196202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418790
SamplesAK1
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
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)nsv819187
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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