A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv707n145



Internal ID22813723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38814837..38817534hg38UCSC Ensembl
chr21:40186761..40189458hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg382698
hg192698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115702, nsv3112905
Samplessample379, sample78, sample375, sample398
Known GenesETS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv707n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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