A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084567



Internal ID21993800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46978065..46978065hg38UCSC Ensembl
chr16:47011976..47011976hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084567
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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