A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586299



Internal ID20959370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118214738..118215323hg38UCSC Ensembl
chr12:118652543..118653128hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229933
Samples
Known GenesTAOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586299
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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