A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670510



Internal ID9936615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20583105..20584840hg38UCSC Ensembl
chr11:20604651..20606386hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381736
hg191736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5767104, essv6536184, essv6414513
SamplesHG01183, HG01171, HG00126
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670510
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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