A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666308



Internal ID9932413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111344423..111349815hg38UCSC Ensembl
Outerchr11:111344386..111349865hg38UCSC Ensembl
Innerchr11:111215148..111220540hg19UCSC Ensembl
Outerchr11:111215111..111220590hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg385480
hg195480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5800115
SamplesNA18560
Known GenesMIR4491
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666308
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