A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618916



Internal ID21567221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126283878..126283878hg38UCSC Ensembl
chr3:126002721..126002721hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121778
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618916
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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