A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935352



Internal ID22710692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66486385..66492234hg38UCSC Ensembl
chr16:66520288..66526137hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385850
hg195850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386065
Samples
Known GenesBEAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935352
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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