A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068961



Internal ID20636001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49125685..49126575hg38UCSC Ensembl
chr20:47742222..47743112hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553278
Supporting Variants
Samples
Known GenesSTAU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00458


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