A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512388



Internal ID15851813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:24870938..24873589hg38UCSC Ensembl
Outerchr15:25116085..25118736hg19UCSC Ensembl
Outerchr15:22667178..22669829hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382652
hg192652
hg182652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624976
Samples1
Known GenesSNRPN
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512388
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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