A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873869



Internal ID22648818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29465794..29472275hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386482
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873869
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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