A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21883



Internal ID15833680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4291207..4292020hg38UCSC Ensembl
Outerchr11:4291180..4292893hg38UCSC Ensembl
Innerchr11:4312437..4313250hg19UCSC Ensembl
Outerchr11:4312410..4314123hg19UCSC Ensembl
Innerchr11:4269013..4269826hg18UCSC Ensembl
Outerchr11:4268986..4270699hg18UCSC Ensembl
Innerchr11:4269013..4269826hg17UCSC Ensembl
Outerchr11:4268986..4270699hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381714
hg191714
hg181714
hg171714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8777
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)nssv21883
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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