A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14384767



Internal ID22278083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89567507..89567574hg38UCSC Ensembl
chr14:90033851..90033918hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223151
Supporting Variants
SamplesNA19239
Known GenesFOXN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14384767
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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