A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8838



Internal ID15846750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:74421006..74430254hg38UCSC Ensembl
Outerchr11:74132051..74141299hg19UCSC Ensembl
Outerchr11:73809699..73818947hg18UCSC Ensembl
Outerchr11:73809699..73818947hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg389249
hg199249
hg189249
hg179249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23053, nssv20649, nssv19866, nssv19112, nssv19856, nssv22333, nssv19314, nssv20164, nssv20917, nssv20335, nssv18311, nssv20208, nssv25361, nssv20918, nssv22926, nssv22808, nssv19970, nssv22381, nssv20043, nssv23779, nssv23275, nssv21238, nssv18130, nssv18412, nssv20235
SamplesNA18502, NA11830, NA18980, NA07029, NA18504, NA12155, NA12802, NA18860, NA18942, NA07048, NA10839, NA18975, NA19007, NA10863, NA12872, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19240, NA19144, NA12740, NA18972
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)nsv8838
Frequency
Sample Size31
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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