A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18924



Internal ID15840108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2862850..2863405hg38UCSC Ensembl
Outerchr11:2862153..2864050hg38UCSC Ensembl
Innerchr11:2884080..2884635hg19UCSC Ensembl
Outerchr11:2883383..2885280hg19UCSC Ensembl
Innerchr11:2840656..2841211hg18UCSC Ensembl
Outerchr11:2839959..2841856hg18UCSC Ensembl
Innerchr11:2840656..2841211hg17UCSC Ensembl
Outerchr11:2839959..2841856hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381898
hg191898
hg181898
hg171898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8765
Supporting Variants
SamplesNA18975
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)nssv18924
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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