A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8n145



Internal ID22813024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17527255..17537349hg38UCSC Ensembl
chr1:17853751..17863844hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3810095
hg1910094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3118340, nsv3115091
Samplessample176, sample339
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv8n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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