A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819583



Internal ID15237548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57093320..57093992hg38UCSC Ensembl
Innerchr3:57127348..57128020hg19UCSC Ensembl
Innerchr3:57102388..57103060hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38673
hg19673
hg18673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419050
SamplesAK1
Known GenesIL17RD
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)nsv819583
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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