A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22039



Internal ID15490576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:128306..168972hg38UCSC Ensembl
Outerchr19:122262..177093hg38UCSC Ensembl
Innerchr19:128306..168972hg19UCSC Ensembl
Outerchr19:122262..177093hg19UCSC Ensembl
Innerchr19:79306..119972hg18UCSC Ensembl
Outerchr19:73262..128093hg18UCSC Ensembl
Innerchr19:79306..119972hg17UCSC Ensembl
Outerchr19:73262..128093hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3854832
hg1954832
hg1854832
hg1754832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9651
Supporting Variants
SamplesNA18572
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)nssv22039
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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