A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512399



Internal ID15851824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:67111894..67113559hg38UCSC Ensembl
Outerchr15:67404232..67405897hg19UCSC Ensembl
Outerchr15:65191286..65192951hg18UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg381666
hg191666
hg181666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624989
Samples1
Known GenesSMAD3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512399
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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