A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8834



Internal ID15500060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:61282109..61296169hg38UCSC Ensembl
Outerchr11:61049581..61063641hg19UCSC Ensembl
Outerchr11:60806157..60820217hg18UCSC Ensembl
Outerchr11:60806157..60820217hg17UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3814061
hg1914061
hg1814061
hg1714061
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19996, nssv22720
SamplesNA18502, NA18552
Known GenesVWCE
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)nsv8834
Frequency
Sample Size31
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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