A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288779



Internal ID20497997
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 StatusS
Merged Variantsnsv4754420
Supporting Variants
Samples
Known GenesSTMN3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288779
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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