A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14258103



Internal ID834959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103626547..103627457hg38UCSC Ensembl
Innerchr11:103626550..103627454hg38UCSC Ensembl
Outerchr11:103626544..103627460hg38UCSC Ensembl
chr11:103497275..103498185hg19UCSC Ensembl
Innerchr11:103497278..103498182hg19UCSC Ensembl
Outerchr11:103497272..103498188hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627562
Supporting Variants
SamplesHG00422
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14258103
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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