A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083547



Internal ID21992780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50414371..50414371hg38UCSC Ensembl
chr16:50448282..50448282hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083547
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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