A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9671



Internal ID15500897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15666486..15723022hg38UCSC Ensembl
Outerchr19:15777296..15833832hg19UCSC Ensembl
Outerchr19:15638296..15694832hg18UCSC Ensembl
Outerchr19:15638296..15694832hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3856537
hg1956537
hg1856537
hg1756537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25604, nssv25627, nssv27701
SamplesNA18860, NA19173
Known GenesCYP4F12
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)nsv9671
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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