A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096538



Internal ID22005771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88086997..88086997hg38UCSC Ensembl
chr16:88120603..88120603hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096538
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer