A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv569n145



Internal ID22813585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39538298..39540804hg38UCSC Ensembl
chr19:40028938..40031444hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382507
hg192507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117564, nsv3112539, nsv3117096
Samplessample196, sample182, sample289, sample86
Known GenesEID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv569n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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