A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1491660



Internal ID12308096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89362686..89362746hg38UCSC Ensembl
chr14:89829030..89829090hg19UCSC Ensembl
chr14:88898783..88898843hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3861
hg1961
hg1861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3995008
SamplesHuRef
Known GenesFOXN3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1491660
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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