A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15090011



Internal ID6604684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86058278..86072205hg38UCSC Ensembl
Innerchr14:86058278..86072205hg38UCSC Ensembl
Outerchr14:86057778..86072705hg38UCSC Ensembl
chr14:86524622..86538549hg19UCSC Ensembl
Innerchr14:86524622..86538549hg19UCSC Ensembl
Outerchr14:86524122..86539049hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3813928
hg1913928
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635219
Supporting Variants
SamplesNA20773
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15090011
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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