A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23307



Internal ID15842021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107369195..107371331hg38UCSC Ensembl
Outerchr11:107368625..107371739hg38UCSC Ensembl
Innerchr11:107239921..107242057hg19UCSC Ensembl
Outerchr11:107239351..107242465hg19UCSC Ensembl
Innerchr11:106745131..106747267hg18UCSC Ensembl
Outerchr11:106744561..106747675hg18UCSC Ensembl
Innerchr11:106745131..106747267hg17UCSC Ensembl
Outerchr11:106744561..106747675hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383115
hg193115
hg183115
hg173115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8872
Supporting Variants
SamplesNA19132
Known GenesCWF19L2
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)nssv23307
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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