A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043399



Internal ID20610439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63287432..63288059hg38UCSC Ensembl
chr18:60954665..60955292hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519075
Supporting Variants
Samples
Known GenesBCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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