A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237094



Internal ID20804134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:38629735..41866813hg38UCSC Ensembl
chr12:39023537..42260615hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg383237079
hg193237079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591997
Supporting Variants
Samples
Known GenesABCD2, C12orf40, CNTN1, CPNE8, KIF21A, LRRK2, MUC19, PDZRN4, SLC2A13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237094
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