A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241867



Internal ID20808907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72149874..72150194hg38UCSC Ensembl
chr15:72442215..72442535hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241867
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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