A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4588e59



Internal ID22765808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49157255..49162986hg38UCSC Ensembl
chrX:49012650..49019548hg19UCSC Ensembl
chrX:48899594..48906492hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg385732
hg196899
hg186899
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3323542, esv3415998
SamplesNA12878
Known GenesMAGIX
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4588e59
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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