A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066231



Internal ID20633271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10403380..10403764hg38UCSC Ensembl
chr20:10384028..10384412hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527488
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00123


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