A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21896



Internal ID15841100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24481939..24492435hg38UCSC Ensembl
Outerchr15:24478321..24492627hg38UCSC Ensembl
Innerchr15:24727086..24737582hg19UCSC Ensembl
Outerchr15:24723468..24737774hg19UCSC Ensembl
Innerchr15:22278179..22288675hg18UCSC Ensembl
Outerchr15:22274561..22288867hg18UCSC Ensembl
Innerchr15:22278179..22288675hg17UCSC Ensembl
Outerchr15:22274561..22288867hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3814307
hg1914307
hg1814307
hg1714307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA19007
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)nssv21896
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