A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581090



Internal ID20954161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118254806..118255904hg38UCSC Ensembl
chr12:118692611..118693709hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1705n223
Supporting Variantsnssv18218434
Samples
Known GenesTAOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581090
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