A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1095n223



Internal ID22804063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48963559..49863338hg38UCSC Ensembl
chr11:48985111..49884890hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38899780
hg19899780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6578528, nsv6585658, nsv6576832
Samples
Known GenesFOLH1, LOC440040, TRIM49B, TRIM64C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1095n223
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