A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622059



Internal ID21814106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32123209..32123209hg38UCSC Ensembl
chr20:30711012..30711012hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105655
Supporting Variants
Samples
Known GenesTM9SF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622059
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