A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272564



Internal ID20481782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35580695..35580695hg38UCSC Ensembl
chr20:34168617..34168617hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272564
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