A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5n199



Internal ID22802891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29394327..30656490hg38UCSC Ensembl
chr1:29720839..31129337hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg381262164
hg191408499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4765174, nsv4767570, nsv4760859
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv5n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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