A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095511



Internal ID22004744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92551940..92551940hg38UCSC Ensembl
chr9:95314222..95314222hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588005
Samples
Known GenesCENPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095511
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