A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671662



Internal ID9591081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:883923..889918hg38UCSC Ensembl
Outerchr11:883886..889968hg38UCSC Ensembl
Innerchr11:883923..889918hg19UCSC Ensembl
Outerchr11:883886..889968hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg386083
hg196083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6554081
SamplesHG00242
Known GenesCHID1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671662
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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