A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220312



Internal ID20787352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71702472..71702926hg38UCSC Ensembl
chr12:72096252..72096706hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577251
Supporting Variants
Samples
Known GenesTMEM19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220312
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