A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221152



Internal ID20788192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122410017..122411196hg38UCSC Ensembl
chr12:122894564..122895743hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381180
hg191180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590355
Supporting Variants
Samples
Known GenesCLIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221152
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