A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819098



Internal ID15583799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141445519..141446306hg38UCSC Ensembl
Innerchr3:141164361..141165148hg19UCSC Ensembl
Innerchr3:142647051..142647838hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38788
hg19788
hg18788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419084
SamplesAK1
Known GenesZBTB38
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)nsv819098
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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