A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4926n223



Internal ID22807894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77262883..77263941hg38UCSC Ensembl
chr3:77312034..77313092hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6538743, nsv6542715
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4926n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer