A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635292



Internal ID6675405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89229670..89231541hg38UCSC Ensembl
Innerchr14:89229685..89231527hg38UCSC Ensembl
Outerchr14:89229656..89231556hg38UCSC Ensembl
chr14:89696014..89697885hg19UCSC Ensembl
Innerchr14:89696029..89697871hg19UCSC Ensembl
Outerchr14:89696000..89697900hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg381872
hg191872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15093025
SamplesNA19307
Known GenesFOXN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635292
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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