A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19376



Internal ID15841361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4291207..4292007hg38UCSC Ensembl
Outerchr11:4291180..4292020hg38UCSC Ensembl
Innerchr11:4312437..4313237hg19UCSC Ensembl
Outerchr11:4312410..4313250hg19UCSC Ensembl
Innerchr11:4269013..4269813hg18UCSC Ensembl
Outerchr11:4268986..4269826hg18UCSC Ensembl
Innerchr11:4269013..4269813hg17UCSC Ensembl
Outerchr11:4268986..4269826hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38841
hg19841
hg18841
hg17841
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8777
Supporting Variants
SamplesNA19007
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)nssv19376
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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