A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1137n223



Internal ID22804105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50655401..50821300hg38UCSC Ensembl
chr11:50614572..50780471hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38165900
hg19165900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6455858, nsv6459967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1137n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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