A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675287



Internal ID9941392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75646914..75648460hg38UCSC Ensembl
Outerchr11:75646757..75648613hg38UCSC Ensembl
Innerchr11:75357959..75359505hg19UCSC Ensembl
Outerchr11:75357802..75359658hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg381857
hg191857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6250838
SamplesNA19213
Known GenesMAP6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675287
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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