A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7461n223



Internal ID22810429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112680238..112681348hg38UCSC Ensembl
chr8:113692467..113693577hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg381111
hg191111
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6569773, nsv6556874
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7461n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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