A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv193e199



Internal ID20123495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12886154..12887406hg38UCSC Ensembl
chr11:12907701..12908953hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381253
hg191253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2661233, esv2678964
SamplesNA19082
Known GenesTEAD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv193e199
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