A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18860



Internal ID15837479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47612997..47697486hg38UCSC Ensembl
Innerchr10:49011943..49095491hg19UCSC Ensembl
Innerchr10:48631949..48715497hg18UCSC Ensembl
Innerchr10:48631949..48715497hg17UCSC Ensembl
Outerchr10:48631403..48865564hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3884490
hg1983549
hg1883549
hg17234162
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)nssv18860
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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