A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14384010



Internal ID22279759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14276848..14276902hg38UCSC Ensembl
chr16:14370705..14370759hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221445
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14384010
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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