A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513113



Internal ID15852535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:758007..759973hg38UCSC Ensembl
Outerchr4:751795..753761hg19UCSC Ensembl
Outerchr4:741795..743761hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381967
hg191967
hg181967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626604
Samples1
Known GenesPCGF3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513113
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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