A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23626



Internal ID15830174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41810364..41810928hg38UCSC Ensembl
Outerchr15:41809427..41811792hg38UCSC Ensembl
Innerchr15:42102562..42103126hg19UCSC Ensembl
Outerchr15:42101625..42103990hg19UCSC Ensembl
Innerchr15:39889854..39890418hg18UCSC Ensembl
Outerchr15:39888917..39891282hg18UCSC Ensembl
Innerchr15:39889854..39890418hg17UCSC Ensembl
Outerchr15:39888917..39891282hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382366
hg192366
hg182366
hg172366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9243
Supporting Variants
SamplesNA11830
Known GenesMAPKBP1
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)nssv23626
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