A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8592



Internal ID15846504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:47285..88355hg38UCSC Ensembl
Outerchr10:93225..134295hg19UCSC Ensembl
Outerchr10:83225..124295hg18UCSC Ensembl
Outerchr10:83225..124295hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3841071
hg1941071
hg1841071
hg1741071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23282
SamplesNA19221
Known GenesTUBB8
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)nsv8592
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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