A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453305



Internal ID21110858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117353793..117376922hg38UCSC Ensembl
chr9:120116072..120139201hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3823130
hg1923130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225523
Samples
Known GenesASTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453305
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