A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626106



Internal ID7012940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42251288..42254226hg38UCSC Ensembl
Innerchr11:42251288..42254226hg38UCSC Ensembl
Outerchr11:42251251..42254274hg38UCSC Ensembl
chr11:42272838..42275776hg19UCSC Ensembl
Innerchr11:42272838..42275776hg19UCSC Ensembl
Outerchr11:42272801..42275824hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382939
hg192939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14109636
SamplesNA19399
Known GenesLOC100507205
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626106
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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