A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883451



Internal ID22658430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:28597536..28600623hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383088
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483940, nssv17483939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883451
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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