A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513658



Internal ID15853079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87924957..87936393hg38UCSC Ensembl
Outerchr4:88846109..88857545hg19UCSC Ensembl
Outerchr4:89065133..89076569hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3811437
hg1911437
hg1811437
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv44n50
Supporting Variantsnssv626910
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513658
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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