A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183414



Internal ID20750454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27819557..27825339hg38UCSC Ensembl
chr9:27819555..27825337hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg385783
hg195783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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