A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27701



Internal ID15491543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15668815..15722624hg38UCSC Ensembl
Outerchr19:15667434..15723022hg38UCSC Ensembl
Innerchr19:15779625..15833434hg19UCSC Ensembl
Outerchr19:15778244..15833832hg19UCSC Ensembl
Innerchr19:15640625..15694434hg18UCSC Ensembl
Outerchr19:15639244..15694832hg18UCSC Ensembl
Innerchr19:15640625..15694434hg17UCSC Ensembl
Outerchr19:15639244..15694832hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3855589
hg1955589
hg1855589
hg1755589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9671
Supporting Variants
SamplesNA18860
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)nssv27701
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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