A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5740568



Internal ID8920333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67478697..67480876hg38UCSC Ensembl
Outerchr11:67478660..67480926hg38UCSC Ensembl
Innerchr11:67246168..67248347hg19UCSC Ensembl
Outerchr11:67246131..67248397hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382267
hg192267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664357
Supporting Variants
SamplesHG00421
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5740568
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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