A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808858



Internal ID13646215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39249383..39266247hg38UCSC Ensembl
Innerchr19:39251373..39264667hg38UCSC Ensembl
Outerchr19:39249273..39266367hg38UCSC Ensembl
chr19:39740023..39756887hg19UCSC Ensembl
Innerchr19:39742013..39755307hg19UCSC Ensembl
Outerchr19:39739913..39757007hg19UCSC Ensembl
chr19:44431863..44448727hg18UCSC Ensembl
Innerchr19:44433853..44447147hg18UCSC Ensembl
Outerchr19:44431753..44448847hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3816865
hg1916865
hg1816865
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3449620
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808858
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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