A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv12204



Internal ID15840041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26453160..26460462hg38UCSC Ensembl
Outerchr4:26452257..26461335hg38UCSC Ensembl
Innerchr4:26454782..26462084hg19UCSC Ensembl
Outerchr4:26453879..26462957hg19UCSC Ensembl
Innerchr4:26063880..26071182hg18UCSC Ensembl
Outerchr4:26062977..26072055hg18UCSC Ensembl
Innerchr4:26131051..26138353hg17UCSC 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 StatusS
Merged Variantsnsv10468
Supporting Variants
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)nssv12204
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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