A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv27n50



Internal ID22767856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:138246286..138251596hg38UCSC Ensembl
chr2:139003856..139009166hg19UCSC Ensembl
chr2:138720326..138725636hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg385311
hg195311
hg185311
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv513643, nsv513644
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)dgv27n50
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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