A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666465



Internal ID9585884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133449566..133453003hg38UCSC Ensembl
chr11:133319461..133322898hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383438
hg193438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5490528, essv5424374, essv5787740, essv6269155, essv6099627
SamplesNA19390, NA19398, HG01136, NA19138, NA19446
Known GenesOPCML
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666465
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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