A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv324n206



Internal ID22755628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:22099191..22899568hg38UCSC Ensembl
chr22:22453601..23241748hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38800378
hg19788148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6146348, nsv6146884
Samples
Known GenesBMS1P20, GGTLC2, IGLL5, LOC648691, MIR650, POM121L1P, PRAME, VPREB1, ZNF280A, ZNF280B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv324n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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