A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3415998



Internal ID15262957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49157790..49162986hg38UCSC Ensembl
InnerchrX:49159372..49161939hg38UCSC Ensembl
OuterchrX:49157670..49162986hg38UCSC Ensembl
chrX:49012650..49018789hg19UCSC Ensembl
InnerchrX:49014640..49017209hg19UCSC Ensembl
OuterchrX:49012540..49018909hg19UCSC Ensembl
chrX:48899594..48905733hg18UCSC Ensembl
InnerchrX:48901584..48904153hg18UCSC Ensembl
OuterchrX:48899484..48905853hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg385197
hg196140
hg186140
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4588e59
Supporting Variantsessv8809620
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3415998
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