A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv217e199



Internal ID18982271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61881645..61885775hg38UCSC Ensembl
chr11:61649117..61653247hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg384131
hg194131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2657647, esv2666997
SamplesNA19471
Known GenesFADS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv217e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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