A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419812



Internal ID15583596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45026702..45033940hg38UCSC Ensembl
Innerchr15:45318900..45326138hg19UCSC Ensembl
Innerchr15:43106192..43113430hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg387239
hg197239
hg187239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820141
Supporting Variants
SamplesAK1
Known GenesSORD
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)nssv1419812
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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