A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819698



Internal ID15237663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:58689725..58691583hg38UCSC Ensembl
Innerchr1:59155397..59157255hg19UCSC Ensembl
Innerchr1:58927985..58929843hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg381859
hg191859
hg181859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419344
SamplesAK1
Known GenesMYSM1
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)nsv819698
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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