A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115822



Internal ID21299088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11579712..11583416hg38UCSC Ensembl
Innerchr18:11579711..11583415hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383705
hg193705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv511n145
Supporting Variantsnssv14100018
Samplessample196
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115822
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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