A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563438



Internal ID336372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30938072..30950110hg38UCSC Ensembl
chr18:28518038..28530076hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3812039
hg1912039
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563438
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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