A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105944



Internal ID21486721
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 StatusS
Merged Variantsnsv5598491
Supporting Variants
SamplesNA12878
Known GenesTNNI3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105944
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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