A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239727



Internal ID20806767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78480458..78481667hg38UCSC Ensembl
chr15:78772800..78774009hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381210
hg191210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588274
Supporting Variants
Samples
Known GenesIREB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239727
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