A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9652903



Internal ID14911714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63067814..63067833hg38UCSC Ensembl
Innerchr11:63067810..63067837hg38UCSC Ensembl
Outerchr11:63067791..63067856hg38UCSC Ensembl
chr11:62835286..62835305hg19UCSC Ensembl
Innerchr11:62835282..62835309hg19UCSC Ensembl
Outerchr11:62835263..62835328hg19UCSC Ensembl
chr11:62591862..62591881hg18UCSC Ensembl
Innerchr11:62591885..62591858hg18UCSC Ensembl
Outerchr11:62591839..62591904hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3410563
Supporting Variants
SamplesNA19143
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9652903
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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