A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819947



Internal ID15584648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2105056..2111045hg38UCSC Ensembl
Innerchr10:2147250..2153239hg19UCSC Ensembl
Innerchr10:2137250..2143239hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg385990
hg195990
hg185990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419750
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)nsv819947
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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