A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8853



Internal ID15846765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:88881201..88931319hg38UCSC Ensembl
Outerchr11:88614369..88664487hg19UCSC Ensembl
Outerchr11:88254017..88304135hg18UCSC Ensembl
Outerchr11:88254017..88304135hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3850119
hg1950119
hg1850119
hg1750119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19946, nssv23303, nssv20399, nssv22483, nssv18529, nssv20537, nssv18160, nssv20133, nssv22513, nssv20295, nssv23098, nssv19172, nssv22471, nssv23040, nssv18485, nssv21298, nssv20978, nssv19926, nssv20238, nssv20030, nssv20116, nssv19404, nssv18472
SamplesNA07029, NA18504, NA12155, NA18563, NA12802, NA18942, NA07048, NA18975, NA19007, NA10847, NA10863, NA18572, NA18537, NA18853, NA18517, NA18564, NA19240, NA19144, NA19173, NA18972, NA18552
Known GenesGRM5
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)nsv8853
Frequency
Sample Size31
Observed Gain21
Observed Loss0
Observed Complex0
Frequencyn/a


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