A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8827



Internal ID15500053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:55599690..55701112hg38UCSC Ensembl
Outerchr11:55367166..55468588hg19UCSC Ensembl
Outerchr11:55123742..55225164hg18UCSC Ensembl
Outerchr11:55123742..55225164hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38101423
hg19101423
hg18101423
hg17101423
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040, nssv19836, nssv20118, nssv18395, nssv18352, nssv19736, nssv22632, nssv20145, nssv19876, nssv23667, nssv20275, nssv20447, nssv18281, nssv23725, nssv20134, nssv25286, nssv20013
SamplesNA18502, NA18980, NA18563, NA12802, NA18860, NA18942, NA07048, NA10839, NA19007, NA10847, NA10863, NA12872, NA19221, NA18537, NA18564, NA18552
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
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)nsv8827
Frequency
Sample Size31
Observed Gain1
Observed Loss16
Observed Complex0
Frequencyn/a


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