A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879812



Internal ID22654782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63478300..63516432hg38UCSC Ensembl
chr16:63512204..63550336hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3838133
hg1938133
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879812
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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