A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22848



Internal ID15839564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5862146..5871366hg38UCSC Ensembl
Outerchr11:5861518..5871982hg38UCSC Ensembl
Innerchr11:5883376..5892596hg19UCSC Ensembl
Outerchr11:5882748..5893212hg19UCSC Ensembl
Innerchr11:5839952..5849172hg18UCSC Ensembl
Outerchr11:5839324..5849788hg18UCSC Ensembl
Innerchr11:5839952..5849172hg17UCSC Ensembl
Outerchr11:5839324..5849788hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810465
hg1910465
hg1810465
hg1710465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8786
Supporting Variants
SamplesNA18972
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)nssv22848
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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