A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv61n145



Internal ID22813077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105492629..105718087hg38UCSC Ensembl
chr1:106035251..106260709hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38225459
hg19225459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115319, nsv3113635
Samplessample319, sample241
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv61n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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