A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626109



Internal ID7012943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42333093..42339592hg38UCSC Ensembl
Innerchr11:42333094..42339591hg38UCSC Ensembl
Outerchr11:42333092..42339593hg38UCSC Ensembl
chr11:42354643..42361142hg19UCSC Ensembl
Innerchr11:42354644..42361141hg19UCSC Ensembl
Outerchr11:42354642..42361143hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14109652
SamplesHG02651
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626109
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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