A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15259



Internal ID15490189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73540..178483hg38UCSC Ensembl
Outerchr8:72957..186606hg38UCSC Ensembl
Innerchr8:23540..128483hg19UCSC Ensembl
Outerchr8:22957..136606hg19UCSC Ensembl
Innerchr8:13540..118483hg18UCSC Ensembl
Outerchr8:12957..126606hg18UCSC Ensembl
Innerchr8:13540..118483hg17UCSC Ensembl
Outerchr8:12957..126606hg17UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38113650
hg19113650
hg18113650
hg17113650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8253
Supporting Variants
SamplesNA18572
Known GenesOR4F21
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)nssv15259
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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