A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8761



Internal ID15499987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:979333..983986hg38UCSC Ensembl
Outerchr11:979333..983986hg19UCSC Ensembl
Outerchr11:969333..973986hg18UCSC Ensembl
Outerchr11:969333..973986hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384654
hg194654
hg184654
hg174654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17680, nssv19725, nssv19653, nssv22244, nssv18692, nssv20109, nssv21703
SamplesNA07029, NA18504, NA12802, NA07048, NA18537, NA18517, NA12740
Known GenesAP2A2
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)nsv8761
Frequency
Sample Size31
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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