A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673103



Internal ID9939208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61991844..61992405hg38UCSC Ensembl
Outerchr11:61991807..61992455hg38UCSC Ensembl
Innerchr11:61759316..61759877hg19UCSC Ensembl
Outerchr11:61759279..61759927hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5754584
SamplesNA19700
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673103
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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