A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4255n223



Internal ID22807223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202288547..202290106hg38UCSC Ensembl
chr2:203153270..203154829hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381560
hg191560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6548302, nsv6543568
Samples
Known GenesNOP58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4255n223
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