A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587320



Internal ID21535879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55159745..55159818hg38UCSC Ensembl
chr19:55671113..55671186hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105947
SamplesHG03065
Known GenesDNAAF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587320
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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