A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14058672



Internal ID1604393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24354196..24486284hg38UCSC Ensembl
Innerchr11:24354247..24486234hg38UCSC Ensembl
Outerchr11:24354146..24486335hg38UCSC Ensembl
chr11:24375742..24507830hg19UCSC Ensembl
Innerchr11:24375793..24507780hg19UCSC Ensembl
Outerchr11:24375692..24507881hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38132089
hg19132089
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625669
Supporting Variants
SamplesHG01491
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14058672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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