A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21733



Internal ID15833350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1059258..1060008hg38UCSC Ensembl
Outerchr11:1058209..1060729hg38UCSC Ensembl
Innerchr11:1059258..1060008hg19UCSC Ensembl
Outerchr11:1058209..1060729hg19UCSC Ensembl
Innerchr11:1049258..1050008hg18UCSC Ensembl
Outerchr11:1048209..1050729hg18UCSC Ensembl
Innerchr11:1049258..1050008hg17UCSC Ensembl
Outerchr11:1048209..1050729hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382521
hg192521
hg182521
hg172521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8762
Supporting Variants
SamplesNA18504
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)nssv21733
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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