A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25627



Internal ID15496545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15678267..15722624hg38UCSC Ensembl
Outerchr19:15675580..15723022hg38UCSC Ensembl
Innerchr19:15789077..15833434hg19UCSC Ensembl
Outerchr19:15786390..15833832hg19UCSC Ensembl
Innerchr19:15650077..15694434hg18UCSC Ensembl
Outerchr19:15647390..15694832hg18UCSC Ensembl
Innerchr19:15650077..15694434hg17UCSC Ensembl
Outerchr19:15647390..15694832hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3847443
hg1947443
hg1847443
hg1747443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9671
Supporting Variants
SamplesNA19173
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)nssv25627
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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