A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274029



Internal ID20483247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63641832..63642014hg38UCSC Ensembl
chr20:62273185..62273367hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734382
Supporting Variants
Samples
Known GenesSTMN3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274029
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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