A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626527



Internal ID7013359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58908765..58913607hg38UCSC Ensembl
Innerchr11:58908799..58913573hg38UCSC Ensembl
Outerchr11:58908731..58913641hg38UCSC Ensembl
chr11:58676238..58681080hg19UCSC Ensembl
Innerchr11:58676272..58681046hg19UCSC Ensembl
Outerchr11:58676204..58681114hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg384843
hg194843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14174279, essv14174280, essv14174278
SamplesNA20853, NA21094, NA20888
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626527
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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