A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22731



Internal ID15839560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4304863..4305397hg38UCSC Ensembl
Outerchr11:4304326..4315056hg38UCSC Ensembl
Innerchr11:4326093..4326627hg19UCSC Ensembl
Outerchr11:4325556..4336286hg19UCSC Ensembl
Innerchr11:4282669..4283203hg18UCSC Ensembl
Outerchr11:4282132..4292862hg18UCSC Ensembl
Innerchr11:4282669..4283203hg17UCSC Ensembl
Outerchr11:4282132..4292862hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810731
hg1910731
hg1810731
hg1710731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8777
Supporting Variants
SamplesNA18972
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)nssv22731
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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