A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7861n223



Internal ID22810829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83168495..83169908hg38UCSC Ensembl
chr9:85783410..85784823hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381414
hg191414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6566526, nsv6555634
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7861n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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