A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv12898



Internal ID15842793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184237555..184246148hg38UCSC Ensembl
Outerchr4:184236394..184250120hg38UCSC Ensembl
Innerchr4:185158708..185167301hg19UCSC Ensembl
Outerchr4:185157547..185171273hg19UCSC Ensembl
Innerchr4:185395702..185404295hg18UCSC Ensembl
Outerchr4:185394541..185408267hg18UCSC Ensembl
Innerchr4:185533857..185542450hg17UCSC Ensembl
Outerchr4:185532696..185546422hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3813727
hg1913727
hg1813727
hg1713727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10623
Supporting Variants
SamplesNA19144
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)nssv12898
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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