A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10529



Internal ID15498806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:86054725..86059733hg38UCSC Ensembl
Outerchr4:86975878..86980886hg19UCSC Ensembl
Outerchr4:87194902..87199910hg18UCSC Ensembl
Outerchr4:87333057..87338065hg17UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg385009
hg195009
hg185009
hg175009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv12661, nssv13191, nssv13407, nssv11675, nssv12037
SamplesNA10847, NA18860, NA19132, NA11830, NA19240
Known GenesMAPK10
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)nsv10529
Frequency
Sample Size31
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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