A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9492



Internal ID15847404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:11134540..11194389hg38UCSC Ensembl
Outerchr17:11037857..11097706hg19UCSC Ensembl
Outerchr17:10978582..11038431hg18UCSC Ensembl
Outerchr17:10978582..11038431hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3859850
hg1959850
hg1859850
hg1759850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28167
SamplesNA19221
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)nsv9492
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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