A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10468



Internal ID15845431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:26452257..26461335hg38UCSC Ensembl
Outerchr4:26453879..26462957hg19UCSC Ensembl
Outerchr4:26062977..26072055hg18UCSC Ensembl
Outerchr4:26130148..26139226hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg389079
hg199079
hg189079
hg179079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv12204
SamplesNA18975
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)nsv10468
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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