A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587424



Internal ID21535984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9877538..9877909hg38UCSC Ensembl
chr18:9877535..9877906hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103104
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587424
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