A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225947



Internal ID20792987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121222220..121223286hg38UCSC Ensembl
chr12:121660023..121661089hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381067
hg191067
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591129
Supporting Variants
Samples
Known GenesP2RX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225947
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