A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21132



Internal ID15832614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47406173..47418344hg38UCSC Ensembl
Outerchr10:47405446..47419415hg38UCSC Ensembl
Innerchr10:48321018..48333189hg19UCSC Ensembl
Outerchr10:48319947..48333916hg19UCSC Ensembl
Innerchr10:47941024..47953195hg18UCSC Ensembl
Outerchr10:47939953..47953922hg18UCSC Ensembl
Innerchr10:47941024..47953195hg17UCSC Ensembl
Outerchr10:47939953..47953922hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3813970
hg1913970
hg1813970
hg1713970
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18502
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)nssv21132
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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