A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560760



Internal ID21885115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170170464..170171751hg38UCSC Ensembl
chr5:169597468..169598755hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381288
hg191288
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106881
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560760
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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