A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239731



Internal ID20806771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78599788..78600394hg38UCSC Ensembl
chr15:78892130..78892736hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591322
Supporting Variants
Samples
Known GenesCHRNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239731
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