A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626583



Internal ID7013415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61496201..61501818hg38UCSC Ensembl
Innerchr11:61496201..61501818hg38UCSC Ensembl
Outerchr11:61495868..61501917hg38UCSC Ensembl
chr11:61263673..61269290hg19UCSC Ensembl
Innerchr11:61263673..61269290hg19UCSC Ensembl
Outerchr11:61263340..61269389hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg385618
hg195618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14178516, essv14178517, essv14178515, essv14178518
SamplesNA18962, NA19000, NA18953, NA18983
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626583
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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