A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24821



Internal ID15840764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14737295..14745974hg38UCSC Ensembl
Outerchr18:14736668..14746476hg38UCSC Ensembl
Innerchr18:14737294..14745973hg19UCSC Ensembl
Outerchr18:14736667..14746475hg19UCSC Ensembl
Innerchr18:14727294..14735973hg18UCSC Ensembl
Outerchr18:14726667..14736475hg18UCSC Ensembl
Innerchr18:14727294..14735973hg17UCSC Ensembl
Outerchr18:14726667..14736475hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg389809
hg199809
hg189809
hg179809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9617
Supporting Variants
SamplesNA18980
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)nssv24821
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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