A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533153



Internal ID20906514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:40440388..40440438hg38UCSC Ensembl
chr18:38020352..38020402hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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