A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601283



Internal ID21549928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22474175..22487262hg38UCSC Ensembl
chr18:20054138..20067225hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3813088
hg1913088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100633
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601283
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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