A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594355



Internal ID20967426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110255629..110256050hg38UCSC Ensembl
chr12:110693434..110693855hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594355
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