A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14189789



Internal ID3148311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65323729..65331202hg38UCSC Ensembl
Innerchr11:65323729..65331202hg38UCSC Ensembl
Outerchr11:65323522..65331412hg38UCSC Ensembl
chr11:65091200..65098673hg19UCSC Ensembl
Innerchr11:65091200..65098673hg19UCSC Ensembl
Outerchr11:65090993..65098883hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387474
hg197474
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626672
Supporting Variants
SamplesHG02772
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14189789
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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