A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190



Internal ID15485158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90098240..90109406hg38UCSC Ensembl
Outerchr11:90096839..90109512hg38UCSC Ensembl
Innerchr11:89831408..89842574hg19UCSC Ensembl
Outerchr11:89830007..89842680hg19UCSC Ensembl
Innerchr11:89471056..89482222hg18UCSC Ensembl
Outerchr11:89469655..89482328hg18UCSC Ensembl
Innerchr11:89471056..89482222hg17UCSC Ensembl
Outerchr11:89469655..89482328hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3812674
hg1912674
hg1812674
hg1712674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8859
Supporting Variants
SamplesNA12802
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)nssv18190
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer