A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1650n223



Internal ID22804618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92671805..92672568hg38UCSC Ensembl
chr12:93065581..93066344hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38764
hg19764
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6584042, nsv6590635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1650n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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