A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5799481



Internal ID9490187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61100013..61100136hg38UCSC Ensembl
Outerchr11:61099976..61100186hg38UCSC Ensembl
Innerchr11:60867485..60867608hg19UCSC Ensembl
Outerchr11:60867448..60867658hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663388
Supporting Variants
SamplesNA18964
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5799481
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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