A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1088n145



Internal ID22814104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169063796..169069398hg38UCSC Ensembl
chr6:169463891..169469493hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg385603
hg195603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116468, nsv3113554
Samplessample78, sample418
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1088n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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