A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024



Internal ID15840122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46707014..46783863hg38UCSC Ensembl
Innerchr10:48105976..48182818hg19UCSC Ensembl
Innerchr10:47725982..47802824hg18UCSC Ensembl
Innerchr10:47725982..47802824hg17UCSC Ensembl
Outerchr10:47575187..47804241hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3876850
hg1976843
hg1876843
hg17229055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18975
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)nssv18024
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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