A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634100



Internal ID7020904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37853872..37862586hg38UCSC Ensembl
Innerchr14:37853872..37862586hg38UCSC Ensembl
Outerchr14:37853780..37862655hg38UCSC Ensembl
chr14:38323077..38331791hg19UCSC Ensembl
Innerchr14:38323077..38331791hg19UCSC Ensembl
Outerchr14:38322985..38331860hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg388715
hg198715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14970166
SamplesHG04006
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634100
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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