A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963598



Internal ID22738533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:28561077..28561374hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399608
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963598
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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