A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3443158



Internal ID14943425
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 StatusM
Merged Variants
Supporting Variantsessv8808497
SamplesNA12878
Known GenesENKUR
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3443158
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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