A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19773



Internal ID15828025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4289549..4292893hg38UCSC Ensembl
Outerchr11:4289504..4293301hg38UCSC Ensembl
Innerchr11:4310779..4314123hg19UCSC Ensembl
Outerchr11:4310734..4314531hg19UCSC Ensembl
Innerchr11:4267355..4270699hg18UCSC Ensembl
Outerchr11:4267310..4271107hg18UCSC Ensembl
Innerchr11:4267355..4270699hg17UCSC Ensembl
Outerchr11:4267310..4271107hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383798
hg193798
hg183798
hg173798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8777
Supporting Variants
SamplesNA07048
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)nssv19773
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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