A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239023



Internal ID20806063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42830195..42830821hg38UCSC Ensembl
chr15:43122393..43123019hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593241
Supporting Variants
Samples
Known GenesTTBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239023
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