A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096114



Internal ID22005347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23504293..23504293hg38UCSC Ensembl
chr9:23504291..23504291hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096114
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