A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15093033



Internal ID5094849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89461292..89471150hg38UCSC Ensembl
Innerchr14:89461292..89471150hg38UCSC Ensembl
Outerchr14:89460792..89471650hg38UCSC Ensembl
chr14:89927636..89937494hg19UCSC Ensembl
Innerchr14:89927636..89937494hg19UCSC Ensembl
Outerchr14:89927136..89937994hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg389859
hg199859
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635295
Supporting Variants
SamplesNA20811
Known GenesFOXN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15093033
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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