A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766584



Internal ID20542444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98041800..98041800hg38UCSC Ensembl
chr15:98585029..98585029hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766584
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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