A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv89n145



Internal ID22813105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178974087..179005655hg38UCSC Ensembl
chr1:178943222..178974790hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3831569
hg1931569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112475, nsv3117867
Samplessample350, sample206, sample169, sample397, sample194
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv89n145
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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