A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1206899



Internal ID12023337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89360824..89360944hg38UCSC Ensembl
chr14:89827168..89827288hg19UCSC Ensembl
chr14:88896921..88897041hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38121
hg19121
hg18121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3705750
SamplesHuRef
Known GenesFOXN3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1206899
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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