A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598491



Internal ID21547118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55155437..55155544hg38UCSC Ensembl
chr19:55666805..55666912hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105944
SamplesNA12878
Known GenesTNNI3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598491
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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