A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068806



Internal ID20635846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37911769..37913387hg38UCSC Ensembl
chr20:36540171..36541789hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381619
hg191619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518072
Supporting Variants
Samples
Known GenesVSTM2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068806
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