A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8560



Internal ID15499786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112842363..112846632hg38UCSC Ensembl
Outerchr9:115604643..115608912hg19UCSC Ensembl
Outerchr9:114644464..114648733hg18UCSC Ensembl
Outerchr9:112684198..112688467hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg384270
hg194270
hg184270
hg174270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18348
SamplesNA18564
Known GenesSNX30
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)nsv8560
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