A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442426



Internal ID21099979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47642201..47713200hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3871000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv726n223
Supporting Variantsnssv18195854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442426
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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