A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676081



Internal ID9942186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10346443..10349303hg38UCSC Ensembl
Outerchr11:10346406..10349353hg38UCSC Ensembl
Innerchr11:10367990..10370850hg19UCSC Ensembl
Outerchr11:10367953..10370900hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382948
hg192948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6104193
SamplesNA20768
Known GenesCAND1.11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676081
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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