A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241933



Internal ID20808973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74394114..74395859hg38UCSC Ensembl
chr15:74686454..74688200hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381746
hg191747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576296
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241933
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