A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874478



Internal ID22649430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38592683..38598584hg38UCSC Ensembl
chr20:37221326..37227227hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg385902
hg195902
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874478
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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