A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1690n223



Internal ID22804658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110237197..110237763hg38UCSC Ensembl
chr12:110675002..110675568hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6592290, nsv6578765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1690n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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