A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10459



Internal ID15845422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:15719720..15722959hg38UCSC Ensembl
Outerchr4:15721343..15724582hg19UCSC Ensembl
Outerchr4:15330441..15333680hg18UCSC Ensembl
Outerchr4:15397612..15400851hg17UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg383240
hg193240
hg183240
hg173240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11938, nssv13063
SamplesNA18504, NA19144
Known GenesBST1
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)nsv10459
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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