A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664646



Internal ID9930751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81738421..82053192hg38UCSC Ensembl
chr11:81449463..81764234hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38314772
hg19314772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5402276
SamplesNA12763
Known GenesMIR4300
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664646
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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