A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668112



Internal ID9934217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4487758..4541167hg38UCSC Ensembl
chr11:4508988..4562397hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3853410
hg1953410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6188937, essv6050747
SamplesNA18599, NA18566
Known GenesOR52K1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668112
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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