A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17285



Internal ID15828901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46736506..46782415hg38UCSC Ensembl
Outerchr10:46736235..46782804hg38UCSC Ensembl
Innerchr10:48135442..48181362hg19UCSC Ensembl
Outerchr10:48135171..48181752hg19UCSC Ensembl
Innerchr10:47755448..47801368hg18UCSC Ensembl
Outerchr10:47755177..47801758hg18UCSC Ensembl
Innerchr10:47755448..47801368hg17UCSC Ensembl
Outerchr10:47755177..47801758hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3846570
hg1946582
hg1846582
hg1746582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA10847
Known GenesCTSLP2
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)nssv17285
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