A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593650



Internal ID20966721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93300435..93301576hg38UCSC Ensembl
chr12:93694211..93695352hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381142
hg191142
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229707
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593650
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