A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635232



Internal ID7022031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86419742..86505993hg38UCSC Ensembl
Innerchr14:86419766..86505970hg38UCSC Ensembl
Outerchr14:86419719..86506017hg38UCSC Ensembl
chr14:86886086..86972337hg19UCSC Ensembl
Innerchr14:86886110..86972314hg19UCSC Ensembl
Outerchr14:86886063..86972361hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3886252
hg1986252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15091136
SamplesHG03851
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635232
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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