A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv198n145



Internal ID22813214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35222398..35238346hg38UCSC Ensembl
chr11:35243945..35259893hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3815949
hg1915949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116574, nsv3113810, nsv3110684
Samplessample133, sample90, sample380, sample420, sample400, sample390, sample278
Known GenesCD44
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv198n145
Frequency
Sample Size467
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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