A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627940



Internal ID7014765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122406764..122410794hg38UCSC Ensembl
Innerchr11:122406772..122410786hg38UCSC Ensembl
Outerchr11:122406756..122410802hg38UCSC Ensembl
chr11:122277472..122281502hg19UCSC Ensembl
Innerchr11:122277480..122281494hg19UCSC Ensembl
Outerchr11:122277464..122281510hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg384031
hg194031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14295782
SamplesHG00118
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627940
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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