A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579402



Internal ID21771445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135518668..135518668hg38UCSC Ensembl
chr9:138410514..138410514hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6098114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579402
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