A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14298447



Internal ID22257540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:26340085..26348365hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388281
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222507
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14298447
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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