A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370193



Internal ID22137610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32018229..32025033hg38UCSC Ensembl
chr14:32487435..32494239hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg386805
hg196805
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230311
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370193
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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