A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178699



Internal ID20745739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3511141..3511696hg38UCSC Ensembl
chr9:3511141..3511696hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420686
Supporting Variants
Samples
Known GenesRFX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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