A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24826



Internal ID15843887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1208843..1262481hg38UCSC Ensembl
Outerchr11:1208218..1263522hg38UCSC Ensembl
Innerchr11:1230073..1283711hg19UCSC Ensembl
Outerchr11:1229448..1284752hg19UCSC Ensembl
Innerchr11:1186649..1240287hg18UCSC Ensembl
Outerchr11:1186024..1241328hg18UCSC Ensembl
Innerchr11:1186649..1240287hg17UCSC Ensembl
Outerchr11:1186024..1241328hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3855305
hg1955305
hg1855305
hg1755305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8763
Supporting Variants
SamplesNA19221
Known GenesMIR6744, MUC5B
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)nssv24826
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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