A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626730



Internal ID7013560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68000461..68000987hg38UCSC Ensembl
Innerchr11:68000502..68000947hg38UCSC Ensembl
Outerchr11:68000421..68001028hg38UCSC Ensembl
chr11:67767931..67768457hg19UCSC Ensembl
Innerchr11:67767972..67768417hg19UCSC Ensembl
Outerchr11:67767891..67768498hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14200055
SamplesNA20886
Known GenesUNC93B1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626730
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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