A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv484n145



Internal ID22813500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19866890..19868956hg38UCSC Ensembl
chr17:19770203..19772269hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382067
hg192067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113286, nsv3117652, nsv3114069
Samplessample289, sample224, sample361, sample33, sample86
Known GenesULK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv484n145
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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