A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7733723



Internal ID14148262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118947969..118947970hg38UCSC Ensembl
Outerchr11:118947794..118948145hg38UCSC Ensembl
Innerchr11:118818679..118818680hg19UCSC Ensembl
Outerchr11:118818504..118818855hg19UCSC Ensembl
Innerchr11:118323890..118323889hg18UCSC Ensembl
Outerchr11:118323714..118324065hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38352
hg19352
hg18352
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303036
Supporting Variants
SamplesNA18944
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7733723
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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