A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307380



Internal ID15154328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10967421..10967422hg38UCSC Ensembl
Innerchr10:10967389..10967454hg38UCSC Ensembl
Outerchr10:10967388..10967455hg38UCSC Ensembl
chr10:11009384..11009385hg19UCSC Ensembl
Innerchr10:11009352..11009417hg19UCSC Ensembl
Outerchr10:11009351..11009418hg19UCSC Ensembl
chr10:11049390..11049391hg18UCSC Ensembl
Innerchr10:11049423..11049358hg18UCSC Ensembl
Outerchr10:11049357..11049424hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38224
hg19224
hg18224
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7750509, essv7745478, essv7763048
SamplesNA18907, NA19257, NA19147
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307380
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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