A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819139



Internal ID15237104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52311467..52313569hg38UCSC Ensembl
Innerchr15:52603664..52605766hg19UCSC Ensembl
Innerchr15:50390956..50393058hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg382103
hg192103
hg182103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419384
SamplesAK1
Known GenesMYO5A
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)nsv819139
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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