A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294165



Internal ID20503383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127509763..127509763hg38UCSC Ensembl
chr9:130272042..130272042hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763120
Supporting Variants
Samples
Known GenesFAM129B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294165
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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