A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv44n50



Internal ID22767873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87924957..87937549hg38UCSC Ensembl
chr4:88846109..88858701hg19UCSC Ensembl
chr4:89065133..89077725hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3812593
hg1912593
hg1812593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv513659, nsv513658
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)dgv44n50
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer