A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21621



Internal ID15491367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45875012..45892843hg38UCSC Ensembl
Outerchr10:45874616..45893298hg38UCSC Ensembl
Innerchr10:46370460..46388291hg19UCSC Ensembl
Outerchr10:46370064..46388746hg19UCSC Ensembl
Innerchr10:45690466..45708297hg18UCSC Ensembl
Outerchr10:45690070..45708752hg18UCSC Ensembl
Innerchr10:45690466..45708297hg17UCSC Ensembl
Outerchr10:45690070..45708752hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3818683
hg1918683
hg1818683
hg1718683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8631
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)nssv21621
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