A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8771



Internal ID15846683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3361218..3370627hg38UCSC Ensembl
Outerchr11:3382448..3391857hg19UCSC Ensembl
Outerchr11:3339024..3348433hg18UCSC Ensembl
Outerchr11:3339024..3348433hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg389410
hg199410
hg189410
hg179410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21931, nssv22152
SamplesNA18502, NA19240
Known GenesZNF195
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)nsv8771
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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