A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8872



Internal ID15846784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:107357638..107378894hg38UCSC Ensembl
Outerchr11:107228364..107249620hg19UCSC Ensembl
Outerchr11:106733574..106754830hg18UCSC Ensembl
Outerchr11:106733574..106754830hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3821257
hg1921257
hg1821257
hg1721257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv20224, nssv20919, nssv23210, nssv18619, nssv21158, nssv21128, nssv25436, nssv20365, nssv22591, nssv21007, nssv19554, nssv22982, nssv20254, nssv20395, nssv20657, nssv23887, nssv20253, nssv21037, nssv19202, nssv20120, nssv23307, nssv23557, nssv20687
SamplesNA18502, NA11830, NA18980, NA07029, NA12155, NA18563, NA18860, NA07048, NA10839, NA18975, NA18572, NA19221, NA18853, NA19132, NA18517, NA19240, NA12740, NA18972
Known GenesCWF19L2
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)nsv8872
Frequency
Sample Size31
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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