A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8842



Internal ID15846754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:80263295..80279380hg38UCSC Ensembl
Outerchr11:79974339..79990424hg19UCSC Ensembl
Outerchr11:79651987..79668072hg18UCSC Ensembl
Outerchr11:79651987..79668072hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3816086
hg1916086
hg1816086
hg1716086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22837, nssv19344
SamplesNA18502, NA18975
Known Genes
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)nsv8842
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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