A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941468



Internal ID22716892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10001297..10001541hg38UCSC Ensembl
chr20:9981945..9982189hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941468
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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