A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110989



Internal ID21294255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63694880..63703284hg38UCSC Ensembl
Innerchr16:63728784..63737188hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg388405
hg198405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096529
Samplessample335
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110989
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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