A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452731



Internal ID21110284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113111542..113112045hg38UCSC Ensembl
chr9:115873822..115874325hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221621
Samples
Known GenesFAM225B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452731
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