A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880057



Internal ID22655027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18980558..18986206hg38UCSC Ensembl
chr20:18961202..18966850hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg385649
hg195649
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880057
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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