A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659208



Internal ID9925313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100923496..100925551hg38UCSC Ensembl
Outerchr11:100923444..100925602hg38UCSC Ensembl
Innerchr11:100794227..100796282hg19UCSC Ensembl
Outerchr11:100794175..100796333hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382159
hg192159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6328629, essv6252366
SamplesNA19712, HG01082
Known GenesARHGAP42
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659208
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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