A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27359



Internal ID15495175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23373315..23374617hg38UCSC Ensembl
Outerchr19:23372070..23374848hg38UCSC Ensembl
Innerchr19:23556117..23557419hg19UCSC Ensembl
Outerchr19:23554872..23557650hg19UCSC Ensembl
Innerchr19:23347957..23349259hg18UCSC Ensembl
Outerchr19:23346712..23349490hg18UCSC Ensembl
Innerchr19:23347957..23349259hg17UCSC Ensembl
Outerchr19:23346712..23349490hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg382779
hg192779
hg182779
hg172779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9686
Supporting Variants
SamplesNA19132
Known GenesZNF91
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)nssv27359
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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