A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24546



Internal ID15834133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19785367..19938590hg38UCSC Ensembl
Outerchr14:19783868..19938991hg38UCSC Ensembl
Innerchr14:20253526..20406749hg19UCSC Ensembl
Outerchr14:20252027..20407150hg19UCSC Ensembl
Innerchr14:19323366..19476589hg18UCSC Ensembl
Outerchr14:19321867..19476990hg18UCSC Ensembl
Innerchr14:19323366..19476589hg17UCSC Ensembl
Outerchr14:19321867..19476990hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38155124
hg19155124
hg18155124
hg17155124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9117
Supporting Variants
SamplesNA18517
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
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)nssv24546
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