A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14367860



Internal ID22146906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105998765..105998840hg38UCSC Ensembl
chr13:106651114..106651189hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230284
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14367860
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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