A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14376597



Internal ID22232536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34205727..34235556hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3829830
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218219
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14376597
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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