A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26836



Internal ID15833513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34237314..34238273hg38UCSC Ensembl
Outerchr19:34236871..34238936hg38UCSC Ensembl
Innerchr19:34728219..34729178hg19UCSC Ensembl
Outerchr19:34727776..34729841hg19UCSC Ensembl
Innerchr19:39420059..39421018hg18UCSC Ensembl
Outerchr19:39419616..39421681hg18UCSC Ensembl
Innerchr19:39420059..39421018hg17UCSC Ensembl
Outerchr19:39419616..39421681hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382066
hg192066
hg182066
hg172066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9706
Supporting Variants
SamplesNA18504
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)nssv26836
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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