A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419915



Internal ID21077468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15384701..15403700hg38UCSC Ensembl
chr9:15384699..15403698hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3819000
hg1919000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419915
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