A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6504n54



Internal ID20139928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46119100..46125856hg38UCSC Ensembl
chr19:46622357..46629113hg19UCSC Ensembl
chr19:51314197..51320953hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg386757
hg196757
hg186757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579873, nsv579872, nsv579876, nsv579879, nsv579878, nsv579881, nsv579874, nsv579875, nsv579880, nsv579877
Samples
Known GenesIGFL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6504n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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