A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954190



Internal ID22729444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60772784..60779595hg38UCSC Ensembl
chr20:59347840..59354651hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg386812
hg196812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954190
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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