A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv262n206



Internal ID22755566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5548750..5556866hg38UCSC Ensembl
chr2:5688882..5696998hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg388117
hg198117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5451318, nsv5450922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv262n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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