A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627352



Internal ID7014182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95471164..95473547hg38UCSC Ensembl
Innerchr11:95471187..95473525hg38UCSC Ensembl
Outerchr11:95471142..95473570hg38UCSC Ensembl
chr11:95204328..95206711hg19UCSC Ensembl
Innerchr11:95204351..95206689hg19UCSC Ensembl
Outerchr11:95204306..95206734hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382384
hg192384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14243550, essv14243548, essv14243552, essv14243549, essv14243551, essv14243553
SamplesHG02490, HG04200, HG04188, HG03703, HG03849, HG03989
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627352
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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