A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069811



Internal ID18976267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89416855..89417756hg38UCSC Ensembl
chr14:89883199..89884100hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762307
SamplesKWP1
Known GenesFOXN3, FOXN3-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069811
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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