A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8840



Internal ID15846752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:74842816..74847911hg38UCSC Ensembl
Outerchr11:74553861..74558956hg19UCSC Ensembl
Outerchr11:74231509..74236604hg18UCSC Ensembl
Outerchr11:74231509..74236604hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg385096
hg195096
hg185096
hg175096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22363
SamplesNA18504
Known GenesXRRA1
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)nsv8840
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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