A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5637n223



Internal ID22808605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10280833..10282766hg38UCSC Ensembl
chr5:10280945..10282878hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381934
hg191934
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6568789, nsv6573574
Samples
Known GenesCMBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5637n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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