A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238319



Internal ID20805359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41290462..41291191hg38UCSC Ensembl
chr15:41582660..41583389hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595154
Supporting Variants
Samples
Known GenesOIP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238319
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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