A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884074



Internal ID22659056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85319755..85320885hg38UCSC Ensembl
chr16:85353361..85354491hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884074
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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