A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266909



Internal ID20476127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137874697..137874697hg38UCSC Ensembl
chr9:140769149..140769149hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763820
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266909
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