A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048303



Internal ID20615343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47595567..47601236hg38UCSC Ensembl
chr19:48098824..48104493hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg385670
hg195670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048303
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