A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808861



Internal ID13646240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41210562..41216635hg38UCSC Ensembl
Innerchr19:41212552..41215055hg38UCSC Ensembl
Outerchr19:41210452..41216755hg38UCSC Ensembl
chr19:41716467..41722540hg19UCSC Ensembl
Innerchr19:41718457..41720960hg19UCSC Ensembl
Outerchr19:41716357..41722660hg19UCSC Ensembl
chr19:46408307..46414380hg18UCSC Ensembl
Innerchr19:46410297..46412800hg18UCSC Ensembl
Outerchr19:46408197..46414500hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg386074
hg196074
hg186074
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3373940
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808861
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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