A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv567n145



Internal ID22813583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35167717..35174589hg38UCSC Ensembl
chr19:35658620..35665492hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386873
hg196873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114128, nsv3111832
Samplessample313, sample147
Known GenesFXYD5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv567n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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