A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18740



Internal ID15837454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46841819..46860017hg38UCSC Ensembl
Outerchr10:46841475..46860696hg38UCSC Ensembl
Innerchr10:48879345..48897543hg19UCSC Ensembl
Outerchr10:48878666..48897887hg19UCSC Ensembl
Innerchr10:48499351..48517549hg18UCSC Ensembl
Outerchr10:48498672..48517893hg18UCSC Ensembl
Innerchr10:48499351..48517549hg17UCSC Ensembl
Outerchr10:48498672..48517893hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3819222
hg1919222
hg1819222
hg1719222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18853
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)nssv18740
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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