A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8061n152



Internal ID22823764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111903158..111908455hg38UCSC Ensembl
chr6:112224361..112229658hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385298
hg195298
Variant TypeCNV line1 deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3233073, nsv3243109, nsv3247234
SamplesNA19240, HG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8061n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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