A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513167



Internal ID15505903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:138044504..138047172hg38UCSC Ensembl
Outerchr4:138965658..138968326hg19UCSC Ensembl
Outerchr4:139185108..139187776hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg382669
hg192669
hg182669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626663
Samples1
Known GenesLINC00616
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513167
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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