A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611532



Internal ID21559837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98693955..98693955hg38UCSC Ensembl
chr4:99615106..99615106hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137960
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611532
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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