A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14286082



Internal ID22157433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13853851..13854307hg38UCSC Ensembl
chr19:13964665..13965121hg19UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214032
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14286082
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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