A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1459170



Internal ID12275606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89506261..89506310hg38UCSC Ensembl
chr14:89972605..89972654hg19UCSC Ensembl
chr14:89042358..89042407hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3596930
SamplesHuRef
Known GenesFOXN3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1459170
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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