A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102882



Internal ID21286742
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 StatusS
Merged Variantsnsv3114956
Supporting Variants
Samplessample393
Known GenesLILRB4, MIR8061
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102882
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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