A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv221n145



Internal ID22813237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105069591..105099370hg38UCSC Ensembl
chr11:104940318..104970097hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3829780
hg1929780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112173, nsv3116083
Samplessample28, sample61, sample163
Known GenesCARD17
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv221n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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