A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627040



Internal ID7013870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84307506..84316907hg38UCSC Ensembl
Innerchr11:84307556..84316857hg38UCSC Ensembl
Outerchr11:84307403..84317010hg38UCSC Ensembl
chr11:84018549..84027950hg19UCSC Ensembl
Innerchr11:84018599..84027900hg19UCSC Ensembl
Outerchr11:84018446..84028053hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg389402
hg199402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14220563, essv14220564
SamplesHG02512, HG02095
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627040
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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