A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114956



Internal ID21298222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54637815..54664893hg38UCSC Ensembl
Innerchr19:55149266..55176344hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3827079
hg1927079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101398, nssv14102882
Samplessample393, sample318
Known GenesLILRB4, MIR8061
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114956
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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