A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3342687



Internal ID15189672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13922584..13922628hg38UCSC Ensembl
Innerchr11:13922600..13922609hg38UCSC Ensembl
Outerchr11:13922556..13922656hg38UCSC Ensembl
chr11:13944131..13944175hg19UCSC Ensembl
Innerchr11:13944147..13944156hg19UCSC Ensembl
Outerchr11:13944103..13944203hg19UCSC Ensembl
chr11:13900707..13900751hg18UCSC Ensembl
Innerchr11:13900732..13900723hg18UCSC Ensembl
Outerchr11:13900679..13900779hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg385988
hg195988
hg185988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8951571, essv8951572
SamplesNA18519, NA19210
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3342687
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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