A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5565674



Internal ID8543077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12886179..12887380hg38UCSC Ensembl
chr11:12907726..12908927hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661233
Supporting Variants
SamplesNA19082
Known GenesTEAD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5565674
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