A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627110



Internal ID7013940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86927847..86931067hg38UCSC Ensembl
Innerchr11:86928347..86930567hg38UCSC Ensembl
Outerchr11:86926847..86932067hg38UCSC Ensembl
chr11:86638889..86642109hg19UCSC Ensembl
Innerchr11:86639389..86641609hg19UCSC Ensembl
Outerchr11:86637889..86643109hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383221
hg193221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14223504, essv14223503
SamplesHG01176, HG01396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627110
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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