A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754420



Internal ID20530280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63641832..63641832hg38UCSC Ensembl
chr20:62273185..62273185hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288779
Samples
Known GenesSTMN3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754420
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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