A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051



Internal ID15832265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46841978..46860017hg38UCSC Ensembl
Outerchr10:46841819..46860696hg38UCSC Ensembl
Innerchr10:48879345..48897384hg19UCSC Ensembl
Outerchr10:48878666..48897543hg19UCSC Ensembl
Innerchr10:48499351..48517390hg18UCSC Ensembl
Outerchr10:48498672..48517549hg18UCSC Ensembl
Innerchr10:48499351..48517390hg17UCSC Ensembl
Outerchr10:48498672..48517549hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3818878
hg1918878
hg1818878
hg1718878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA12872
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)nssv17051
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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