A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627672



Internal ID7014500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108209178..108217310hg38UCSC Ensembl
Innerchr11:108209226..108217262hg38UCSC Ensembl
Outerchr11:108209130..108217358hg38UCSC Ensembl
chr11:108079905..108088037hg19UCSC Ensembl
Innerchr11:108079953..108087989hg19UCSC Ensembl
Outerchr11:108079857..108088085hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg388133
hg198133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14278403, essv14278402
SamplesHG00583, HG00662
Known GenesNPAT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627672
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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