A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631053



Internal ID21823100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62166667..62166667hg38UCSC Ensembl
chr20:60741723..60741723hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103718
Supporting Variants
Samples
Known GenesSS18L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631053
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer