A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14384210



Internal ID22210053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24851174..24851501hg38UCSC Ensembl
chr16:24862495..24862822hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214379
Supporting Variants
SamplesHG00732
Known GenesSLC5A11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14384210
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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