A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1378771



Internal ID12195208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89361000..89361066hg38UCSC Ensembl
chr14:89827344..89827410hg19UCSC Ensembl
chr14:88897097..88897163hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3867
hg1967
hg1867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3966516
SamplesHuRef
Known GenesFOXN3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1378771
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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