A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107946



Internal ID22017181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:6565893..6565893hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107946
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