A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089975



Internal ID21999208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72806356..72806356hg38UCSC Ensembl
chr9:75421272..75421272hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581722
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089975
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