A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597396



Internal ID21789439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128794520..128795506hg38UCSC Ensembl
chr9:131556799..131557785hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020269
Supporting Variants
Samples
Known GenesTBC1D13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597396
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer