A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5700176



Internal ID9081522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123207815..123208374hg38UCSC Ensembl
chr11:123078523..123079082hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675056
Supporting Variants
SamplesHG01060
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5700176
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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