A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20437



Internal ID15483347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133476534..133480935hg38UCSC Ensembl
Outerchr10:133475414..133481352hg38UCSC Ensembl
Innerchr10:135290038..135294439hg19UCSC Ensembl
Outerchr10:135288918..135294856hg19UCSC Ensembl
Innerchr10:135140028..135144429hg18UCSC Ensembl
Outerchr10:135138908..135144846hg18UCSC Ensembl
Innerchr10:135178919..135183320hg17UCSC Ensembl
Outerchr10:135177799..135183737hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385939
hg195939
hg185939
hg175939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8752
Supporting Variants
SamplesNA11830
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)nssv20437
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer