A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10419



Internal ID15845382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:788528..795026hg38UCSC Ensembl
Outerchr4:782316..788814hg19UCSC Ensembl
Outerchr4:772316..778814hg18UCSC Ensembl
Outerchr4:772146..778644hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg386499
hg196499
hg186499
hg176499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv29193
SamplesNA10863
Known GenesCPLX1
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)nsv10419
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