A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649096



Internal ID21597401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98412831..98412831hg38UCSC Ensembl
chr15:98956060..98956060hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092976
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649096
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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