A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819730



Internal ID15584431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:83811694..84086904hg38UCSC Ensembl
Innerchr2:84038818..84314028hg19UCSC Ensembl
Innerchr2:83892329..84167539hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38275211
hg19275211
hg18275211
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6n43
Supporting Variantsnssv1418800
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)nsv819730
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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