A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578730



Internal ID21770773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109396883..109400860hg38UCSC Ensembl
chr9:112159163..112163140hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg383978
hg193978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009987
Supporting Variants
Samples
Known GenesPTPN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578730
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