A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658899



Internal ID9925004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:123444085..123449694hg38UCSC Ensembl
Outerchr11:123443928..123449847hg38UCSC Ensembl
Innerchr11:123314793..123320402hg19UCSC Ensembl
Outerchr11:123314636..123320555hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg385920
hg195920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5404555, essv6181808, essv6397872, essv5985610
SamplesHG00543, HG00500, HG00704, NA18541
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658899
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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