A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22131



Internal ID15838216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46748544..46755651hg38UCSC Ensembl
Outerchr10:46748033..46756093hg38UCSC Ensembl
Innerchr10:48147487..48154603hg19UCSC Ensembl
Outerchr10:48146976..48155045hg19UCSC Ensembl
Innerchr10:47767493..47774609hg18UCSC Ensembl
Outerchr10:47766982..47775051hg18UCSC Ensembl
Innerchr10:47767493..47774609hg17UCSC Ensembl
Outerchr10:47766982..47775051hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg388061
hg198070
hg188070
hg178070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18860
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)nssv22131
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