A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7444n223



Internal ID22810412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103992121..103993118hg38UCSC Ensembl
chr8:105004349..105005346hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6564492, nsv6562295
Samples
Known GenesRIMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7444n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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