A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819853



Internal ID15237818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:161984411..161985018hg38UCSC Ensembl
Innerchr2:162840921..162841528hg19UCSC Ensembl
Innerchr2:162549167..162549774hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38608
hg19608
hg18608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419023
SamplesAK1
Known GenesSLC4A10
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)nsv819853
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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