A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954



Internal ID15481697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15378274..15380374hg38UCSC Ensembl
Outerchr8:15377765..15381890hg38UCSC Ensembl
Innerchr8:15235783..15237883hg19UCSC Ensembl
Outerchr8:15235274..15239399hg19UCSC Ensembl
Innerchr8:15280154..15282254hg18UCSC Ensembl
Outerchr8:15279645..15283770hg18UCSC Ensembl
Innerchr8:15280154..15282254hg17UCSC Ensembl
Outerchr8:15279645..15283770hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg384126
hg194126
hg184126
hg174126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8298
Supporting Variants
SamplesNA10839
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)nssv16954
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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