A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17255



Internal ID15828931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46707014..46727038hg38UCSC Ensembl
Innerchr10:48105976..48125983hg19UCSC Ensembl
Innerchr10:47725982..47745989hg18UCSC Ensembl
Innerchr10:47725982..47745989hg17UCSC Ensembl
Outerchr10:47575187..47746041hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3820025
hg1920008
hg1820008
hg17170855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA10847
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)nssv17255
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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