A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882005



Internal ID22656982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22665889..22675445hg38UCSC Ensembl
chr20:22646527..22656083hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg389557
hg199557
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882005
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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