A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv109n145



Internal ID22813125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209934665..209941275hg38UCSC Ensembl
chr1:210108010..210114620hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg386611
hg196611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116891, nsv3111046, nsv3111726
Samplessample300, sample397, sample296
Known GenesSYT14
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv109n145
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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