A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095660



Internal ID22004893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121891961..121891961hg38UCSC Ensembl
chr9:124654240..124654240hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581315
Samples
Known GenesTTLL11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095660
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