A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8753



Internal ID15846665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:60001..107470hg38UCSC Ensembl
Outerchr11:60001..107470hg19UCSC Ensembl
Outerchr11:50001..97470hg18UCSC Ensembl
Outerchr11:43964..97470hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3847470
hg1947470
hg1847470
hg1753507
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23189, nssv21613, nssv19665, nssv17929, nssv19684
SamplesNA18504, NA18860, NA10839, NA18572, NA18537
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)nsv8753
Frequency
Sample Size31
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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