A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14287276



Internal ID22200774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19521332..19521620hg38UCSC Ensembl
chr19:19632141..19632429hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226425
Supporting Variants
SamplesHG00732
Known GenesNDUFA13
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14287276
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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