A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1614n223



Internal ID22804582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75110956..75112001hg38UCSC Ensembl
chr12:75504736..75505781hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg381046
hg191046
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6586097, nsv6581797
Samples
Known GenesKCNC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1614n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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