A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003658



Internal ID7068763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54215069..54257872hg38UCSC Ensembl
Innerchr19:54718938..54761735hg19UCSC Ensembl
Innerchr19:59410750..59453547hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3842804
hg1942798
hg1842798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586012
SamplesHuRef
Known GenesLILRA6, LILRB3, LILRB5
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003658
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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