A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947284



Internal ID22722787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22445240..22447071hg38UCSC Ensembl
chr18:20025203..20027034hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381832
hg191832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387916
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947284
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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