A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761186



Internal ID20537046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54220446..54220446hg38UCSC Ensembl
chr16:54254358..54254358hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761186
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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