A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266570



Internal ID20475788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40298239..40298239hg38UCSC Ensembl
chr20:38926879..38926879hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266570
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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