A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1722n223



Internal ID22804690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122906407..122907200hg38UCSC Ensembl
chr12:123390954..123391747hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6594547, nsv6586625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1722n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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