A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14373585



Internal ID22138970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95138937..95139010hg38UCSC Ensembl
chr14:95605274..95605347hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223652
Supporting Variants
SamplesHG00513
Known GenesDICER1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14373585
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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