A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886071



Internal ID22661057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89305659..89310440hg38UCSC Ensembl
chr16:89372067..89376848hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg384782
hg194782
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474728, nssv17479768
Samples
Known GenesANKRD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886071
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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