A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14250877



Internal ID1933360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100410128..100522832hg38UCSC Ensembl
Innerchr11:100410155..100522805hg38UCSC Ensembl
Outerchr11:100410101..100522859hg38UCSC Ensembl
chr11:100280859..100393563hg19UCSC Ensembl
Innerchr11:100280886..100393536hg19UCSC Ensembl
Outerchr11:100280832..100393590hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38112705
hg19112705
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627481
Supporting Variants
SamplesHG01801
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14250877
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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