A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4272n223



Internal ID22807240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207593245..207593853hg38UCSC Ensembl
chr2:208457969..208458577hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6549484, nsv6555342
Samples
Known GenesCREB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4272n223
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