A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873877



Internal ID22648826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18261695..18266294hg38UCSC Ensembl
chr20:18242339..18246938hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483227
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873877
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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