A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8954889



Internal ID14560583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123371079..123371086hg38UCSC Ensembl
Innerchr11:123371072..123371093hg38UCSC Ensembl
Outerchr11:123371065..123371100hg38UCSC Ensembl
chr11:123241787..123241794hg19UCSC Ensembl
Innerchr11:123241780..123241801hg19UCSC Ensembl
Outerchr11:123241773..123241808hg19UCSC Ensembl
chr11:122746997..122747004hg18UCSC Ensembl
Innerchr11:122747011..122746990hg18UCSC Ensembl
Outerchr11:122746983..122747018hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38222
hg19222
hg18222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3325894
Supporting Variants
SamplesNA18951
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8954889
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