A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428901



Internal ID21086454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32082201..32091800hg38UCSC Ensembl
chr9:32082199..32091798hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7686n223
Supporting Variantsnssv18218949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428901
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