A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21747



Internal ID15841766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48490941..48941736hg17UCSC Ensembl
Outerchr10:48490108..48942528hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17452421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19132
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)nssv21747
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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