A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671584



Internal ID9591003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120788266..120794521hg38UCSC Ensembl
Outerchr11:120788229..120794571hg38UCSC Ensembl
Innerchr11:120658975..120665230hg19UCSC Ensembl
Outerchr11:120658938..120665280hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg386343
hg196343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6205472
SamplesNA18511
Known GenesGRIK4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671584
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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