A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv212n145



Internal ID22813228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75054534..75086715hg38UCSC Ensembl
chr11:74765579..74797760hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3832182
hg1932182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111571, nsv3111175
Samplessample143, sample395
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv212n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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