A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819848



Internal ID15237813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:111432982..111440610hg38UCSC Ensembl
Innerchr1:111975604..111983232hg19UCSC Ensembl
Innerchr1:111777127..111784755hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg387629
hg197629
hg187629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419837
SamplesAK1
Known GenesWDR77
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)nsv819848
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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