A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26843



Internal ID15844145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105476984..105485520hg38UCSC Ensembl
Outerchr14:105476516..105485998hg38UCSC Ensembl
Innerchr14:105943321..105951857hg19UCSC Ensembl
Outerchr14:105942853..105952335hg19UCSC Ensembl
Innerchr14:105014366..105022902hg18UCSC Ensembl
Outerchr14:105013898..105023380hg18UCSC Ensembl
Innerchr14:105014366..105022902hg17UCSC Ensembl
Outerchr14:105013898..105023380hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg389483
hg199483
hg189483
hg179483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9177
Supporting Variants
SamplesNA19221
Known GenesCRIP2
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)nssv26843
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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