A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10296



Internal ID15845259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:103685023..103696656hg38UCSC Ensembl
Outerchr3:103403867..103415500hg19UCSC Ensembl
Outerchr3:104886557..104898190hg18UCSC Ensembl
Outerchr3:104886557..104898190hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3811634
hg1911634
hg1811634
hg1711634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28614
SamplesNA10847
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)nsv10296
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