A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8742



Internal ID15499968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131915051..131921066hg38UCSC Ensembl
Outerchr10:133728555..133734570hg19UCSC Ensembl
Outerchr10:133578545..133584560hg18UCSC Ensembl
Outerchr10:133578545..133584560hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386016
hg196016
hg186016
hg176016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19256, nssv20057, nssv19306, nssv17899
SamplesNA18563, NA18572, NA18552, NA19007
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)nsv8742
Frequency
Sample Size31
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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