A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11n145



Internal ID22813027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25428518..25433523hg38UCSC Ensembl
chr1:25755009..25760014hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385006
hg195006
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116263, nsv3118070
Samplessample365, sample412
Known GenesTMEM57
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv11n145
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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