A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756336



Internal ID20532196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33739656..33739656hg38UCSC Ensembl
chr15:34031857..34031857hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg385916
hg195916
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292814
Samples
Known GenesRYR3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756336
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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