A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1359n223



Internal ID22804327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6267950..6269695hg38UCSC Ensembl
chr12:6377116..6378861hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381746
hg191746
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6580837, nsv6589294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1359n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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