A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv36n50



Internal ID22767865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128627926..128659576hg38UCSC Ensembl
chr3:128346769..128378419hg19UCSC Ensembl
chr3:129829459..129861109hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3831651
hg1931651
hg1831651
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv513652, nsv513651
Samples1
Known GenesRPN1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)dgv36n50
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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