A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674143



Internal ID9593562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94168312..94177105hg38UCSC Ensembl
chr11:93901478..93910271hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388794
hg198794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5966690
SamplesNA19434
Known GenesPANX1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674143
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