A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416295



Internal ID21073848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4370453..4395030hg38UCSC Ensembl
chr9:4370453..4395030hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3824578
hg1924578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer