A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21707



Internal ID15836165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19206882..19232584hg38UCSC Ensembl
Outerchr14:19205978..19232584hg38UCSC Ensembl
Innerchr14:19754823..19780824hg19UCSC Ensembl
Outerchr14:19754140..19781728hg19UCSC Ensembl
Innerchr14:18824823..18850824hg18UCSC Ensembl
Outerchr14:18824140..18851728hg18UCSC Ensembl
Innerchr14:18824823..18850824hg17UCSC Ensembl
Outerchr14:18824140..18851728hg17UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg3826607
hg1927589
hg1827589
hg1727589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9117
Supporting Variants
SamplesNA18563
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)nssv21707
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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