A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090296



Internal ID21999529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93818383..93818383hg38UCSC Ensembl
chr9:96580665..96580665hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090296
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