A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111847



Internal ID21295113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11580038..11583148hg38UCSC Ensembl
Innerchr18:11580037..11583147hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383111
hg193111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv511n145
Supporting Variantsnssv14099571
Samplessample119
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111847
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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