A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626756



Internal ID6666904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69766591..69771810hg38UCSC Ensembl
Innerchr11:69766594..69771807hg38UCSC Ensembl
Outerchr11:69766588..69771813hg38UCSC Ensembl
chr11:69581359..69586578hg19UCSC Ensembl
Innerchr11:69581362..69586575hg19UCSC Ensembl
Outerchr11:69581356..69586581hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg385220
hg195220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14207037
SamplesHG00759
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626756
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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