A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593298



Internal ID20966369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69344367..69348166hg38UCSC Ensembl
chr12:69738147..69741946hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593298
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