A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041635



Internal ID20608675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59802950..59806363hg38UCSC Ensembl
chr18:57470182..57473595hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg383414
hg193414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524121
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041635
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