A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669612



Internal ID9935717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105887194..105939684hg38UCSC Ensembl
Outerchr11:105887157..105939734hg38UCSC Ensembl
Innerchr11:105757920..105810410hg19UCSC Ensembl
Outerchr11:105757883..105810460hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3852578
hg1952578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6539363
SamplesHG00256
Known GenesGRIA4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669612
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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