A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7853n223



Internal ID22810821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81461785..81462444hg38UCSC Ensembl
chr9:84076700..84077359hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6567159, nsv6567199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7853n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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