A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5399970



Internal ID9688689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86636490..86639821hg38UCSC Ensembl
Outerchr11:86636453..86639871hg38UCSC Ensembl
Innerchr11:86347532..86350863hg19UCSC Ensembl
Outerchr11:86347495..86350913hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383419
hg193419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672841
Supporting Variants
SamplesNA19439
Known GenesME3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5399970
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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