A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819395



Internal ID15237360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:65087568..65091059hg38UCSC Ensembl
Innerchr2:65314702..65318193hg19UCSC Ensembl
Innerchr2:65168206..65171697hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383492
hg193492
hg183492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419552
SamplesAK1
Known GenesRAB1A
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)nsv819395
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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