A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870821



Internal ID22645758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21727752..21730124hg38UCSC Ensembl
chr16:21739073..21741445hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg382373
hg192373
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477618, nssv17477619
Samples
Known GenesOTOA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870821
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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