A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv885n145



Internal ID22813901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68303713..68618203hg38UCSC Ensembl
chr4:69169431..69483921hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38314491
hg19314491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117694, nsv3110699
Samplessample180, sample31
Known GenesTMPRSS11E, UGT2B17, YTHDC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv885n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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