A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8727



Internal ID15846639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:115725350..115788244hg38UCSC Ensembl
Outerchr10:117484860..117547755hg19UCSC Ensembl
Outerchr10:117474850..117537745hg18UCSC Ensembl
Outerchr10:117474850..117537745hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3862895
hg1962896
hg1862896
hg1762896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21343
SamplesNA18504
Known GenesATRNL1
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)nsv8727
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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