A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1720n223



Internal ID22804688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122782546..122783017hg38UCSC Ensembl
chr12:123267093..123267564hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6590645, nsv6590583
Samples
Known GenesCCDC62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1720n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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