A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808614



Internal ID13643672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17769003..17858466hg38UCSC Ensembl
Innerchr12:17770993..17856886hg38UCSC Ensembl
Outerchr12:17768893..17858586hg38UCSC Ensembl
chr12:17921937..18011400hg19UCSC Ensembl
Innerchr12:17923927..18009820hg19UCSC Ensembl
Outerchr12:17921827..18011520hg19UCSC Ensembl
chr12:17813204..17902667hg18UCSC Ensembl
Innerchr12:17815194..17901087hg18UCSC Ensembl
Outerchr12:17813094..17902787hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3889464
hg1989464
hg1889464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3432140
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808614
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