A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19935



Internal ID15834855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18929155..18950334hg38UCSC Ensembl
Outerchr11:18928410..18950763hg38UCSC Ensembl
Innerchr11:18950702..18971881hg19UCSC Ensembl
Outerchr11:18949957..18972310hg19UCSC Ensembl
Innerchr11:18907278..18928457hg18UCSC Ensembl
Outerchr11:18906533..18928886hg18UCSC Ensembl
Innerchr11:18907278..18928457hg17UCSC Ensembl
Outerchr11:18906533..18928886hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822354
hg1922354
hg1822354
hg1722354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8795
Supporting Variants
SamplesNA18537
Known GenesMRGPRX1
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)nssv19935
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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