A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594063



Internal ID20967134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110415399..110416788hg38UCSC Ensembl
chr12:110853204..110854593hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg381390
hg191390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594063
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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