A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18386



Internal ID15841464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46707014..46772068hg38UCSC Ensembl
Innerchr10:48105976..48170999hg19UCSC Ensembl
Innerchr10:47725982..47791005hg18UCSC Ensembl
Innerchr10:47725982..47791005hg17UCSC Ensembl
Outerchr10:47575187..47791480hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3865055
hg1965024
hg1865024
hg17216294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19007
Known GenesCTSLP2
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)nssv18386
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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