A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14366068



Internal ID22259625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18420626..18420748hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38123
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220085
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14366068
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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