A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758930



Internal ID20534790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66474547..66474547hg38UCSC Ensembl
chr16:66508450..66508450hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286267
Samples
Known GenesBEAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758930
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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