A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111991



Internal ID21295257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:30393118..30401414hg38UCSC Ensembl
Innerchr5:30393225..30401521hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg388297
hg198297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108469
Samplessample155
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111991
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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