A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454285



Internal ID21111838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92773479..92789053hg38UCSC Ensembl
chr9:95535761..95551335hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3815575
hg1915575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454285
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