A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17230



Internal ID15831807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46707014..46717569hg38UCSC Ensembl
Innerchr10:48105976..48116528hg19UCSC Ensembl
Innerchr10:47725982..47736534hg18UCSC Ensembl
Innerchr10:47725982..47736534hg17UCSC Ensembl
Outerchr10:47575187..47736710hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3810556
hg1910553
hg1810553
hg17161524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA12802
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)nssv17230
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