A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv553n145



Internal ID22813569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15423705..15427392hg38UCSC Ensembl
chr19:15534516..15538203hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383688
hg193688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117620, nsv3114696
Samplessample156, sample227
Known GenesWIZ
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv553n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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