A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10585



Internal ID15845548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:144202394..144204328hg38UCSC Ensembl
Outerchr4:145123547..145125481hg19UCSC Ensembl
Outerchr4:145342997..145344931hg18UCSC Ensembl
Outerchr4:145481152..145483086hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381935
hg191935
hg181935
hg171935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14303
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)nsv10585
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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