A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241932



Internal ID20808972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74388201..74394435hg38UCSC Ensembl
chr15:74680541..74686775hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg386235
hg196235
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241932
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