A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808836



Internal ID13646006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12487237..12492866hg38UCSC Ensembl
Innerchr19:12489227..12491286hg38UCSC Ensembl
Outerchr19:12487127..12492986hg38UCSC Ensembl
chr19:12598051..12603680hg19UCSC Ensembl
Innerchr19:12600041..12602100hg19UCSC Ensembl
Outerchr19:12597941..12603800hg19UCSC Ensembl
chr19:12459051..12464680hg18UCSC Ensembl
Innerchr19:12461041..12463100hg18UCSC Ensembl
Outerchr19:12458941..12464800hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385630
hg195630
hg185630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3385866
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808836
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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