A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670858



Internal ID9936963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42251335..42254211hg38UCSC Ensembl
chr11:42272885..42275761hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382877
hg192877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6315316
SamplesNA19399
Known GenesLOC100507205
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670858
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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