A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14278496



Internal ID3050159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109180883..109190975hg38UCSC Ensembl
Innerchr11:109180883..109190975hg38UCSC Ensembl
Outerchr11:109180827..109191018hg38UCSC Ensembl
chr11:109051610..109061702hg19UCSC Ensembl
Innerchr11:109051610..109061702hg19UCSC Ensembl
Outerchr11:109051554..109061745hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3810093
hg1910093
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627696
Supporting Variants
SamplesHG02682
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14278496
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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