A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3380977



Internal ID14881252
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8808578
SamplesNA12878
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3380977
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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