A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv193n145



Internal ID22813209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16893707..16904889hg38UCSC Ensembl
chr11:16915254..16926436hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811183
hg1911183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112580, nsv3111792
Samplessample312, sample7
Known GenesPLEKHA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv193n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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