A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105140



Internal ID21493891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49363491..49363491hg38UCSC Ensembl
chr19:49866748..49866748hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662356
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105140
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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