A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069019



Internal ID20636059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49779928..49782149hg38UCSC Ensembl
chr20:48396465..48398686hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg382222
hg192222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543550
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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