A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24726



Internal ID15844824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45027681..45031581hg38UCSC Ensembl
Outerchr15:45027008..45031787hg38UCSC Ensembl
Innerchr15:45319879..45323779hg19UCSC Ensembl
Outerchr15:45319206..45323985hg19UCSC Ensembl
Innerchr15:43107171..43111071hg18UCSC Ensembl
Outerchr15:43106498..43111277hg18UCSC Ensembl
Innerchr15:43107171..43111071hg17UCSC Ensembl
Outerchr15:43106498..43111277hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg384780
hg194780
hg184780
hg174780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9259
Supporting Variants
SamplesNA19240
Known GenesSORD
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)nssv24726
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