A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5782n223



Internal ID22808750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67998618..67999801hg38UCSC Ensembl
chr5:67294446..67295629hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg381184
hg191184
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6566249, nsv6573304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5782n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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