A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808497



Internal ID13295746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25008925..25013240hg38UCSC Ensembl
Innerchr10:25010915..25011660hg38UCSC Ensembl
Outerchr10:25008815..25013360hg38UCSC Ensembl
chr10:25297854..25302169hg19UCSC Ensembl
Innerchr10:25299844..25300589hg19UCSC Ensembl
Outerchr10:25297744..25302289hg19UCSC Ensembl
chr10:25337860..25342175hg18UCSC Ensembl
Innerchr10:25339850..25340595hg18UCSC Ensembl
Outerchr10:25337750..25342295hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384316
hg194316
hg184316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3443158
Supporting Variants
SamplesNA12878
Known GenesENKUR
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808497
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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