A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5794950



Internal ID8772353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69969687..69976248hg38UCSC Ensembl
chr11:69815793..69822354hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg386562
hg196562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678418
Supporting Variants
SamplesHG01124
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5794950
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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