A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8809005



Internal ID13652674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49804836..49806714hg38UCSC Ensembl
Innerchr20:49805134..49806715hg38UCSC Ensembl
Outerchr20:49804726..49806834hg38UCSC Ensembl
chr20:48421373..48423251hg19UCSC Ensembl
Innerchr20:48421671..48423252hg19UCSC Ensembl
Outerchr20:48421263..48423371hg19UCSC Ensembl
chr20:47854780..47856658hg18UCSC Ensembl
Innerchr20:47856659..47855078hg18UCSC Ensembl
Outerchr20:47854670..47856778hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg381879
hg191879
hg181879
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3364525
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8809005
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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