A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19294



Internal ID15828287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58007826..58008226hg38UCSC Ensembl
Outerchr10:58007317..58009325hg38UCSC Ensembl
Innerchr10:59767586..59767986hg19UCSC Ensembl
Outerchr10:59767077..59769085hg19UCSC Ensembl
Innerchr10:59437592..59437992hg18UCSC Ensembl
Outerchr10:59437083..59439091hg18UCSC Ensembl
Innerchr10:59437592..59437992hg17UCSC Ensembl
Outerchr10:59437083..59439091hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382009
hg192009
hg182009
hg172009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8677
Supporting Variants
SamplesNA10839
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)nssv19294
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