A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633294



Internal ID21825341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16582225..16691148hg38UCSC Ensembl
chr20:16562870..16671793hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38108924
hg19108924
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042575
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633294
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