A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871587



Internal ID22646525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52540298..52547299hg38UCSC Ensembl
chr16:52574210..52581211hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg387002
hg197002
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471589
Samples
Known GenesTOX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871587
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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