A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9168



Internal ID15500394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:103065392..103446969hg38UCSC Ensembl
Outerchr14:103531729..103913306hg19UCSC Ensembl
Outerchr14:102601482..102983059hg18UCSC Ensembl
Outerchr14:102601482..102983059hg17UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38381578
hg19381578
hg18381578
hg17381578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv20934
SamplesNA18975
Known GenesEIF5, EXOC3L4, LINC00605, MARK3, SNORA28, TNFAIP2
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv9168
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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