A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7829n223



Internal ID22810797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72601344..72602533hg38UCSC Ensembl
chr9:75216260..75217449hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6560649, nsv6563516
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7829n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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