A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv612n145



Internal ID22813628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38375314..38378987hg38UCSC Ensembl
chr2:38602456..38606129hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg383674
hg193674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113062, nsv3116848
Samplessample224, sample59
Known GenesATL2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv612n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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