A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808857



Internal ID13646116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37852542..37856424hg38UCSC Ensembl
Innerchr19:37854532..37854844hg38UCSC Ensembl
Outerchr19:37852432..37856544hg38UCSC Ensembl
chr19:38343182..38347064hg19UCSC Ensembl
Innerchr19:38345172..38345484hg19UCSC Ensembl
Outerchr19:38343072..38347184hg19UCSC Ensembl
chr19:43035022..43038904hg18UCSC Ensembl
Innerchr19:43037012..43037324hg18UCSC Ensembl
Outerchr19:43034912..43039024hg18UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg383883
hg193883
hg183883
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3410769
Supporting Variants
SamplesNA12878
Known GenesLOC100631378
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808857
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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