A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627287



Internal ID7014117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93271147..93281810hg38UCSC Ensembl
Innerchr11:93271174..93281783hg38UCSC Ensembl
Outerchr11:93271120..93281837hg38UCSC Ensembl
chr11:93004313..93014976hg19UCSC Ensembl
Innerchr11:93004340..93014949hg19UCSC Ensembl
Outerchr11:93004286..93015003hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3810664
hg1910664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14236482, essv14236483
SamplesHG01170, HG01088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627287
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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