A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654112



Internal ID21602417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55155786..55155786hg38UCSC Ensembl
chr19:55667154..55667154hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105945
SamplesNA18939
Known GenesTNNI3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654112
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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