A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1421n223



Internal ID22804389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11578527..11579086hg38UCSC Ensembl
chr12:11731461..11732020hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6582506, nsv6586968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1421n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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