A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv269n206



Internal ID22755573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:78036682..78469961hg38UCSC Ensembl
chr2:78263808..78697087hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38433280
hg19433280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5448454, nsv5434643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv269n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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