A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112038



Internal ID21295304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65124544..65127299hg38UCSC Ensembl
Innerchr16:65158447..65161202hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382756
hg192756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098307
Samplessample54
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112038
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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