A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670893



Internal ID9936998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95374413..95376707hg38UCSC Ensembl
Outerchr11:95374376..95376757hg38UCSC Ensembl
Innerchr11:95107577..95109871hg19UCSC Ensembl
Outerchr11:95107540..95109921hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382382
hg192382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5857021
SamplesNA19436
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670893
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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