A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14286416



Internal ID22157556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35703396..35703745hg38UCSC Ensembl
chr19:36194298..36194647hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224971
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14286416
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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