A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25317



Internal ID15483338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23282887..23283571hg38UCSC Ensembl
Outerchr19:23282240..23284221hg38UCSC Ensembl
Innerchr19:23465689..23466373hg19UCSC Ensembl
Outerchr19:23465042..23467023hg19UCSC Ensembl
Innerchr19:23257529..23258213hg18UCSC Ensembl
Outerchr19:23256882..23258863hg18UCSC Ensembl
Innerchr19:23257529..23258213hg17UCSC Ensembl
Outerchr19:23256882..23258863hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381982
hg191982
hg181982
hg171982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9686
Supporting Variants
SamplesNA11830
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)nssv25317
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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