A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5720n152



Internal ID22821423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35389328..35389419hg38UCSC Ensembl
chr22:35785321..35785412hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3295148, nsv3289509
SamplesNA19240, HG00514
Known GenesHMOX1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv5720n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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