A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591166



Internal ID20964237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56374011..56374495hg38UCSC Ensembl
chr12:56767795..56768279hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591166
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