A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14200065



Internal ID3271706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68133010..68140108hg38UCSC Ensembl
Innerchr11:68133160..68139958hg38UCSC Ensembl
Outerchr11:68132860..68140258hg38UCSC Ensembl
chr11:67900477..67907575hg19UCSC Ensembl
Innerchr11:67900627..67907425hg19UCSC Ensembl
Outerchr11:67900327..67907725hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg387099
hg197099
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626733
Supporting Variants
SamplesHG02887
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14200065
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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