A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23815



Internal ID15843490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48869030..48922436hg19UCSC Ensembl
Outerchr10:48868586..48922817hg19UCSC Ensembl
Innerchr10:48489036..48542442hg18UCSC Ensembl
Outerchr10:48488592..48542823hg18UCSC Ensembl
Innerchr10:48489036..48542442hg17UCSC Ensembl
Outerchr10:48488592..48542823hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1954232
hg1854232
hg1754232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19221
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)nssv23815
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