A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15491



Internal ID15485614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15258992..15260865hg38UCSC Ensembl
Outerchr8:15258511..15261463hg38UCSC Ensembl
Innerchr8:15116501..15118374hg19UCSC Ensembl
Outerchr8:15116020..15118972hg19UCSC Ensembl
Innerchr8:15160872..15162745hg18UCSC Ensembl
Outerchr8:15160391..15163343hg18UCSC Ensembl
Innerchr8:15160872..15162745hg17UCSC Ensembl
Outerchr8:15160391..15163343hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg382953
hg192953
hg182953
hg172953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8298
Supporting Variants
SamplesNA12872
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)nssv15491
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer