A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068789



Internal ID20635829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37506723..37516171hg38UCSC Ensembl
chr20:36135125..36144573hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg389449
hg199449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521202
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068789
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