A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103308



Internal ID21412879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13853851..13854306hg38UCSC Ensembl
chr19:13964665..13965120hg19UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596953
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103308
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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