A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1600275



Internal ID12416709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89361163..89361352hg38UCSC Ensembl
chr14:89827507..89827696hg19UCSC Ensembl
chr14:88897260..88897449hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38190
hg19190
hg18190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3944506
SamplesHuRef
Known GenesFOXN3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1600275
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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