A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10769



Internal ID15845732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:166411509..166582158hg38UCSC Ensembl
Outerchr5:165838514..166009163hg19UCSC Ensembl
Outerchr5:165771092..165941741hg18UCSC Ensembl
Outerchr5:165771092..165941741hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38170650
hg19170650
hg18170650
hg17170650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14369, nssv15914
SamplesNA18517, NA19173
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)nsv10769
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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