A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819743



Internal ID15584444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93282075..93286040hg38UCSC Ensembl
Innerchr10:95041832..95045797hg19UCSC Ensembl
Innerchr10:95031822..95035787hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383966
hg193966
hg183966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419594
SamplesAK1
Known Genes
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)nsv819743
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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