A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv191e199



Internal ID20123493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8936445..8943662hg38UCSC Ensembl
chr11:8957992..8965209hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387218
hg197218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2665061, esv2678695
SamplesNA18622
Known GenesASCL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv191e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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