A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1678n223



Internal ID22804646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104157553..104158450hg38UCSC Ensembl
chr12:104551331..104552228hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6595553, nsv6589504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1678n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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