A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9486



Internal ID15847398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:805972..807906hg38UCSC Ensembl
Outerchr17:709212..711146hg19UCSC Ensembl
Outerchr17:655962..657896hg18UCSC Ensembl
Outerchr17:655962..657896hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381935
hg191935
hg181935
hg171935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26771
SamplesNA18517
Known GenesNXN
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)nsv9486
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