A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3304240



Internal ID15151188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:81106351..81106352hg38UCSC Ensembl
Innerchr10:81106309..81106394hg38UCSC Ensembl
Outerchr10:81106308..81106395hg38UCSC Ensembl
chr10:82866107..82866108hg19UCSC Ensembl
Innerchr10:82866065..82866150hg19UCSC Ensembl
Outerchr10:82866064..82866151hg19UCSC Ensembl
chr10:82856087..82856088hg18UCSC Ensembl
Innerchr10:82856130..82856045hg18UCSC Ensembl
Outerchr10:82856044..82856131hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7749148, essv7749562, essv7741046, essv7743846, essv7746051, essv7756388
SamplesNA18856, NA18912, NA18517, NA19240, NA19093, NA18511
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3304240
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer