A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671190



Internal ID9590609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90227996..90280967hg38UCSC Ensembl
Outerchr11:90227959..90281017hg38UCSC Ensembl
Innerchr11:89961164..90014135hg19UCSC Ensembl
Outerchr11:89961127..90014185hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3853059
hg1953059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5492092
SamplesHG00146
Known GenesDISC1FP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671190
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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