A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8836



Internal ID15500062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67985408..68052332hg38UCSC Ensembl
Outerchr11:67752879..67819799hg19UCSC Ensembl
Outerchr11:67509455..67576375hg18UCSC Ensembl
Outerchr11:67509455..67576375hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3866925
hg1966921
hg1866921
hg1766921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25336
SamplesNA19221
Known GenesALDH3B1, MIR4691, MIR6753, MIR7113, NDUFS8, TCIRG1, UNC93B1
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)nsv8836
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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