A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820134



Internal ID15584835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:74377691..74378324hg38UCSC Ensembl
Innerchr2:74604818..74605451hg19UCSC Ensembl
Innerchr2:74458326..74458959hg18UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38634
hg19634
hg18634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419033
SamplesAK1
Known GenesDCTN1
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)nsv820134
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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