A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600158



Internal ID21792205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24601725..24606179hg38UCSC Ensembl
chr14:25070931..25075385hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg384455
hg194455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105750
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600158
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