A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098939



Internal ID22008172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25509620..25509620hg38UCSC Ensembl
chr16:25520941..25520941hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098939
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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