A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590983



Internal ID20964054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93452369..93453397hg38UCSC Ensembl
chr12:93846145..93847173hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230502
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590983
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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