A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv866n223



Internal ID22803834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97472410..97474084hg38UCSC Ensembl
chr10:99232167..99233841hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381675
hg191675
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6587131, nsv6587832
Samples
Known GenesMMS19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv866n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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