A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583603



Internal ID21775646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60575359..60575359hg38UCSC Ensembl
chr9_gl000199_random:56801..56801hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086797
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583603
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