A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18685



Internal ID15840749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46707014..46718840hg38UCSC Ensembl
Innerchr10:48105976..48117796hg19UCSC Ensembl
Innerchr10:47725982..47737802hg18UCSC Ensembl
Innerchr10:47725982..47737802hg17UCSC Ensembl
Outerchr10:47575187..47738392hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3811827
hg1911821
hg1811821
hg17163206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18980
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)nssv18685
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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