A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761800



Internal ID20537660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3889314..3889314hg38UCSC Ensembl
chr16:3939315..3939315hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761800
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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