A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385964



Internal ID22142465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98330527..98330787hg38UCSC Ensembl
chr14:98796864..98797124hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225232
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385964
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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