A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26937



Internal ID15844876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34236871..34238936hg38UCSC Ensembl
Outerchr19:34236108..34240571hg38UCSC Ensembl
Innerchr19:34727776..34729841hg19UCSC Ensembl
Outerchr19:34727013..34731476hg19UCSC Ensembl
Innerchr19:39419616..39421681hg18UCSC Ensembl
Outerchr19:39418853..39423316hg18UCSC Ensembl
Innerchr19:39419616..39421681hg17UCSC Ensembl
Outerchr19:39418853..39423316hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384464
hg194464
hg184464
hg174464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9706
Supporting Variants
SamplesNA19240
Known Genes
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)nssv26937
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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