A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8651



Internal ID15499877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45959155..45960816hg38UCSC Ensembl
Outerchr10:51635022..51636688hg19UCSC Ensembl
Outerchr10:51305028..51306694hg18UCSC Ensembl
Outerchr10:51305028..51306694hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381662
hg191667
hg181667
hg171667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21481
SamplesNA19240
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)nsv8651
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer