A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756226



Internal ID20532086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54378379..54378379hg38UCSC Ensembl
chr16:54412291..54412291hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756226
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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