A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909



Internal ID15836939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46843556..46868354hg38UCSC Ensembl
Outerchr10:46843083..46868427hg38UCSC Ensembl
Innerchr10:46684107..46709274hg19UCSC Ensembl
Outerchr10:46684034..46709748hg19UCSC Ensembl
Innerchr10:46104113..46129280hg18UCSC Ensembl
Outerchr10:46104040..46129754hg18UCSC Ensembl
Innerchr10:46104113..46129280hg17UCSC Ensembl
Outerchr10:46104040..46129754hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3825345
hg1925715
hg1825715
hg1725715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18572
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)nssv16909
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