A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877424



Internal ID22652389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89305761..89320036hg38UCSC Ensembl
chr16:89372169..89386444hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3814276
hg1914276
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474729
Samples
Known GenesANKRD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877424
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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