A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4903n223



Internal ID22807871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68989466..68990417hg38UCSC Ensembl
chr3:69038617..69039568hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38952
hg19952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6536689, nsv6536015
Samples
Known GenesEOGT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4903n223
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