A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582258



Internal ID20955329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54243733..54244306hg38UCSC Ensembl
chr12:54637517..54638090hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221910
Samples
Known GenesCBX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer