A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808578



Internal ID13296592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55596881..55666701hg38UCSC Ensembl
Innerchr11:55598871..55665121hg38UCSC Ensembl
Outerchr11:55596771..55666821hg38UCSC Ensembl
chr11:55364357..55434177hg19UCSC Ensembl
Innerchr11:55366347..55432597hg19UCSC Ensembl
Outerchr11:55364247..55434297hg19UCSC Ensembl
chr11:55120933..55190753hg18UCSC Ensembl
Innerchr11:55122923..55189173hg18UCSC Ensembl
Outerchr11:55120823..55190873hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3869821
hg1969821
hg1869821
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3380977
Supporting Variants
SamplesNA12878
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808578
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