A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580196



Internal ID16367605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54334531hg38UCSC Ensembl
Innerchr19:54731679..54845802hg19UCSC Ensembl
Innerchr19:59423491..59537614hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38106727
hg19114124
hg18114124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6549n54
Supporting Variantsnssv901496
Samples
Known GenesLILRA3, LILRA4, LILRA5, LILRA6, LILRB2, LILRB5, MIR4752
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580196
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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